4.4 Article

The ALLEGRO trial: a placebo controlled randomised trial of intravenous lidocaine in accelerating gastrointestinal recovery after colorectal surgery

Journal

TRIALS
Volume 23, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13063-022-06021-5

Keywords

Colorectal surgery; Minimally invasive surgery; Recovery; Pain; Analgesia; Gastrointestinal; Intravenous lidocaine; Ileus; RCT; Protocol

Funding

  1. NIHR Health and Technology Assessment programme [15/130/95]
  2. University of Edinburgh & Lothian Health Board (ACCORD)
  3. Queen's Medical Research Institute, 47 Little France Crescent, Edinburgh

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The ALLEGRO trial aims to assess the effectiveness of perioperative intravenous lidocaine in improving return of GI function after minimally invasive colorectal surgery. The study suggests that IV lidocaine can accelerate the recovery of GI function, reduce the rate of postoperative ileus, shorten hospital stay, alleviate pain and discomfort, and lead to faster recovery and discharge from hospital, resulting in significant cost savings for the National Health Service (NHS).
Background: Return of gastrointestinal (GI) function is fundamental to patient recovery after colorectal surgery and is required before patients can be discharged from hospital safely. Up to 40% of patients suffer delayed return of GI function after colorectal surgery, causing nausea, vomiting and abdominal discomfort, resulting in longer hospital stay. Small, randomised studies have suggested perioperative intravenous (IV) lidocaine, which has analgesic and anti-inflammatory effects, may accelerate return of GI function after colorectal surgery. The ALLEGRO trial is a pragmatic effectiveness study to assess the benefit of perioperative IV lidocaine in improving return of GI function after elective minimally invasive (laparoscopic or robotic) colorectal surgery. Methods: United Kingdom (UK) multi-centre double blind placebo-controlled randomised controlled trial in 562 patients undergoing elective minimally invasive colorectal resection. IV lidocaine or placebo will be infused for 6-12 h commencing at the start of surgery as an adjunct to usual analgesic/anaesthetic technique. The primary outcome will be return of GI function. Discussion: A 6-12-h perioperative intravenous infusion of 2% lidocaine is a cheap addition to usual anaesthetic/analgesic practice in elective colorectal surgery with a low incidence of adverse side-effects. If successful in achieving quicker return of gut function for more patients, it would reduce the rate of postoperative ileus and reduce the duration of inpatient recovery, resulting in reduced pain and discomfort with faster recovery and discharge from hospital. Since colorectal surgery is a common procedure undertaken in every acute hospital in the UK, a reduced length of stay and reduced rate of postoperative ileus would accrue significant cost savings for the National Health Service (NHS).

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