AHA. Holmberg

A. Holmberg

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


A. Holmberg has a total of 9 co-authors. Here are the top co-authors by number of shared publications:

  • T. Drægni

    Department of Research and Development Division of Emergencies and Critical Care Oslo University Hospital Oslo Norway

    2 shared publications
  • A. Gulestøl

    Department of Anaesthesiology, Oslo University Hospital, Oslo, Norway

    1 shared publication
  • A. Nordby

    Department of Anaesthesiology, Oslo University Hospital, Oslo, Norway

    1 shared publication
  • Axel Rudolf Sauter

    Division of Emergencies and Critical Care, Department of Anaesthesia and Intensive Care Medicine, Oslo University Hospital, Oslo, Norway and Department of Anesthesiology, Bern University Hospital Inselspital, University of Bern, Bern, Switzerland

    1 shared publication
  • F. S. Ottesen

    Department of Anaesthesiology, Oslo University Hospital, Oslo, Norway

    1 shared publication
  • J. C. Ræder

    Department of Anaesthesiology Oslo University Hospital Oslo Norway

    1 shared publication

Latest Publications

  • Analgesic effect of intravenous dexamethasone after volar plate surgery for distal radius fracture with brachial plexus block anaesthesia: a prospective, double‐blind randomised clinical trial *

    by A. Holmberg, S. S. Hassellund, T. Drægni, A. Nordby, F. S. Ottesen, A. Gulestøl, J. Ræder

    Summary: Rebound pain after brachial plexus block resolution and development of long‐lasting pain are problems associated with volar plate fixation for distal radius fractures. The aim of this double‐blind study was to evaluate the effect of a single prophylactic intravenous dose of dexamethasone in this setting. The primary endpoint was highest pain score during the first 24 hours after surgery. We included 51 adults of ASA physical status 1–2 due to undergo planned acute fixation of the radius. All received premedication with oral paracetamol and etoricoxib, and a pre‐operative brachial plexus block with ropivacaine. Patients were randomly allocated into two groups: a dexamethasone group receiving 16 mg dexamethasone intravenously at start of surgery and a control group receiving 4 ml saline. After surgery, all patients received fixed doses of paracetamol, etoricoxib and oxycodone, with further oxycodone added as needed in the first 48 hours. Pain, analgesic consumption and daily function were registered at predefined times up to 1 year after surgery. Median (IQR [range]) worst pain score in the first 24 hours, as assessed by verbal numeric rating scale (0–10), was 4 (2‐6 [0–7]) in the dexamethasone group compared with 8 (5–8 [2–10]) in the placebo group (p < 0.001). Average pain score, 2 (1–4 [0–5]) vs. 5 (3–6 [0–8]), p = 0.001 and rescue oxycodone consumption, 5 (0‐10 [0‐35]) mg vs. 10 (5‐15 [0‐50]) mg, p = 0.037), respectively, were both significantly lower in the dexamethasone group compared with control from 8 to 24 hours. Brachial plexus block duration was 69% longer in the dexamethasone group, 21.5 (19.1‐23.4 [12.9‐24.1]) hours vs. 12.7 (11.9‐15.3 [7.4‐26.6]) hours, p < 0.001. Two patients (9%) in the dexamethasone group compared with 12 (50%) in the placebo group experienced worst pain scores of 8‐10 during the first 36 hours (p = 0.002). At 3 and 7 days postoperatively, there were no significant differences between groups for pain scores or opioid consumption. At 6 months, 27 patients (57%) reported pain at the site of surgery, with significantly higher average pain score (p = 0.024) in the placebo group. At 1 year, two patients in the dexamethasone group reported pain compared with 10 in the placebo group (p = 0.015), and worst pain score was significantly higher in the placebo group (p = 0.018). We conclude that intravenous dexamethasone improves early postoperative analgesia and may also improve clinical outcomes after 6 and 12 months.


  • Pre‐operative brachial plexus block compared with an identical block performed at the end of surgery: a prospective, double‐blind, randomised clinical trial

    by A. Holmberg, A. R. Sauter, Ø. Klaastad, T. Drægni, J. C. Ræder

    Summary: We evaluated whether pre‐emptive analgesia with a pre‐operative ultrasound‐guided infraclavicular brachial plexus block resulted in better postoperative analgesia than an identical block performed postoperatively. Fifty‐two patients undergoing fixation of a fractured radius were included. All patients received general anaesthesia with remifentanil and propofol. Patients were randomly allocated into two groups: a pre‐operative block or a postoperative block with 0.5 ml.kg −1 ropivacaine 0.75%. After surgery, all patients received regular paracetamol plus opioids for breakthrough pain. Mean ( SD ) time to first rescue analgesic after emergence from general anaesthesia was 544 (217) min in the pre‐operative block group compared with 343 (316) min in the postoperative block group (p = 0.015). Postoperative pain scores were higher and more patients required rescue analgesia during the first 4 h after surgery in the postoperative block group. There were no significant differences in plasma stress mediators between the groups. Analgesic consumption was lower at day seven in the pre‐operative block group. Pain was described as very strong at block resolution in 27 (63%) patients and 26 (76%) had episodes of mild pain after 6 months. We conclude that a pre‐operative ultrasound‐guided infraclavicular brachial plexus block provides longer and better analgesia in the acute postoperative period compared with an identical postoperative block in patients undergoing surgery for fractured radius.