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Dexamethasone as an adjuvant for peripheral nerve blockade: a randomised, triple-blinded crossover study in volunteers.
Marhofer, Peter; Columb, Malachy; Hopkins, Phil M; Greher, Manfred; Marhofer, Daniela; Bienzle, Max; Zeitlinger, Markus.
Afiliación
  • Marhofer P; Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Vienna, Austria. Electronic address: peter.marhofer@meduniwien.ac.at.
  • Columb M; Department of Anaesthesia, Manchester University Hospitals Foundation Trust, Wythenshawe, UK.
  • Hopkins PM; Leeds Institute of Medical Research at St James's, University of Leeds, Leeds, UK.
  • Greher M; Department of Anaesthesia, Intensive Care Medicine and Pain Therapy, Herz Jesu Hospital Vienna, Vienna, Austria.
  • Marhofer D; Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Vienna, Austria.
  • Bienzle M; Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Zeitlinger M; Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
Br J Anaesth ; 122(4): 525-531, 2019 Apr.
Article en En | MEDLINE | ID: mdl-30857609
ABSTRACT

BACKGROUND:

The efficacy of dexamethasone in extending the duration of local anaesthetic block is uncertain. In a randomised controlled triple blind crossover study in volunteers, we tested the hypothesis that neither i.v. nor perineurally administered dexamethasone prolongs the sensory block achieved with ropivacaine.

METHODS:

Ultrasound-guided ulnar nerve blocks (ropivacaine 0.75% wt/vol, 3 ml, with saline 1 ml with or without dexamethasone 4 mg) were performed on three occasions in 24 male volunteers along with an i.v. injection of saline 1 ml with or without dexamethasone 4 mg. The combinations of saline and dexamethasone were as follows control group, perineural and i.v. saline; perineural group, perineural dexamethasone and i.v. saline; i.v. group, perineural saline and i.v. dexamethasone. Sensory block was measured using a VAS in response to pinprick testing. The duration of sensory block was the primary outcome and time to onset of sensory block the secondary outcome.

RESULTS:

All 24 subjects completed the trial. The median [inter-quartile range (IQR)] duration of sensory block was 6.87 (5.85-7.62) h in the control group, 7.37 (5.78-7.93) h in the perineural group and 7.37 (6.10-7.97) h in the i.v. group (P=0.61). There was also no significant difference in block onset time between the three groups.

CONCLUSION:

Dexamethasone 4 mg has no clinically relevant effect on the duration of sensory block provided by ropivacaine applied to the ulnar nerve. CLINICAL TRIAL REGISTRATION DRKS, 00014604; EudraCT, 2018-001221-98.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dexametasona / Adyuvantes Anestésicos / Anestésicos Locales / Bloqueo Nervioso Tipo de estudio: Clinical_trials Límite: Adolescent / Adult / Humans / Male / Middle aged Idioma: En Revista: Br J Anaesth Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dexametasona / Adyuvantes Anestésicos / Anestésicos Locales / Bloqueo Nervioso Tipo de estudio: Clinical_trials Límite: Adolescent / Adult / Humans / Male / Middle aged Idioma: En Revista: Br J Anaesth Año: 2019 Tipo del documento: Article