Home > Journals > Minerva Anestesiologica > Past Issues > Minerva Anestesiologica 2014 August;80(8) > Minerva Anestesiologica 2014 August;80(8):954-62

CURRENT ISSUEMINERVA ANESTESIOLOGICA

A Journal on Anesthesiology, Resuscitation, Analgesia and Intensive Care


Official Journal of the Italian Society of Anesthesiology, Analgesia, Resuscitation and Intensive Care
Indexed/Abstracted in: Current Contents/Clinical Medicine, EMBASE, PubMed/MEDLINE, Science Citation Index Expanded (SciSearch), Scopus
Impact Factor 2,036


eTOC

 

EXPERTS’ OPINION  


Minerva Anestesiologica 2014 August;80(8):954-62

language: English

Sedation after cardiac arrest and during therapeutic hypothermia

Dell’Anna A. M. 1, Taccone F. S. 1, Halenarova K. 2, Citerio G. 3

1 Department of Intensive Care, Erasme Hospital, Université Libre de Bruxelles, Route de Lennik, Bruxelles, Belgium;
2 Department of Anesthesiology, Erasme Hospital, Université Libre de Bruxelles, Route de Lennik, Bruxelles, Belgium;
3 Neurointensive Care Unit, San Gerardo Hospital, Monza, Italy


FULL TEXT  REPRINTS


Mild therapeutic hypothermia (MTH) has improved neurological outcome of comatose patients after cardiac arrest (CA). Since the first clinical studies performed in this setting, sedation has always been associated with cooling procedures. The use of sedative drugs during MTH is required because it allows faster achievement and better maintenance of target temperature. Further studies are necessary to prove any potential neuroprotective effects of sedation after CA. No differences in clinical outcomes have been found among different drugs, except for those related to their intrinsic pharmacological properties: the association propofol/remifentanil provides a faster recovery of consciousness than midazolam/fentanyl but is associated with the need of more vasopressors to maintain stable hemodynamic. Moreover, pharmacokinetic properties of these drugs are often altered during MTH so that standard drug regimens could result in overdosing because of reduced clearance. Neuromonitoring could be helpful to titrate drugs’ effects and detect earlier complications (i.e. seizure), while a wake-up test should be avoided during the first 24 hours after CA.

top of page