Research
Print page Print page
Switch language
The Capital Region of Denmark - a part of Copenhagen University Hospital
Published

Sphenopalatine ganglion block for the treatment of postdural puncture headache: a randomised, blinded, clinical trial

Research output: Contribution to journalJournal articleResearchpeer-review

  1. Minimising droplet and virus spread during and after tracheal extubation

    Research output: Contribution to journalLetterResearchpeer-review

  2. Enhanced recovery after surgery components and perioperative outcomes: a nationwide observational study

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Use of the GRADE approach in systematic reviews and guidelines

    Research output: Contribution to journalEditorialResearchpeer-review

  1. Physiological abnormalities in patients admitted with acute exacerbation of COPD: an observational study with continuous monitoring

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Pharmacokinetics of an intravenous bolus dose of clonidine in children undergoing surgery

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Noninvasive respiratory support in the hypoxaemic peri-operative/periprocedural patient: a joint ESA/ESICM guideline

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Noninvasive respiratory support in the hypoxaemic peri-operative/periprocedural patient: A joint ESA/ESICM guideline

    Research output: Contribution to journalJournal articleResearchpeer-review

View graph of relations

BACKGROUND: Current treatment of postdural puncture headache includes epidural blood patch (EBP), which is invasive and may result in rare but severe complications. Sphenopalatine ganglion block is suggested as a simple, minimally invasive treatment for postdural puncture headache. We aimed to investigate the analgesic effect of a transnasal sphenopalatine ganglion block with local anaesthetic vs saline.

METHODS: We conducted a blinded, randomised clinical trial including adults fulfilling the criteria for EBP. Participants received a sphenopalatine ganglion block bilaterally with 1 ml of either local anaesthetic (lidocaine 4% and ropivacaine 0.5%) or placebo (saline). Primary outcome was pain in upright position 30 min post-block, measured on a 0-100 mm VAS.

RESULTS: We randomised 40 patients with an upright median pain intensity of 74 and 84 mm in the local anaesthetic and placebo groups at baseline, respectively. At 30 min after sphenopalatine ganglion block, the median pain intensity in upright position was 26 mm in the local anaesthetic group vs 37 mm in the placebo group (estimated median difference: 5 mm; 95% confidence interval: -14 to 21; P=0.53). In the local anaesthetic group, 50% required an EBP compared with 45% in the placebo group (P=0.76).

CONCLUSIONS: Administration of a sphenopalatine ganglion block with local anaesthetic had no statistically significant effect on pain intensity after 30 min compared with placebo. However, pain was reduced and EBP was avoided in half the patients of both groups, which suggests a major effect not necessarily attributable to local anaesthetics.

CLINICAL TRIAL REGISTRATION: NCT03652714.

Original languageEnglish
JournalBritish Journal of Anaesthesia
Volume124
Issue number6
Pages (from-to)739-747
ISSN0007-0912
DOIs
Publication statusPublished - 2020

ID: 60284659