Objective. The latest European guidelines for the management of hemorrhagic shock suggest the use of vasopressors (norepinephrine) in order to restore an adequate mean arterial pressure when fluid resuscitation therapy fails to restore blood pressure. The administration of arginine vasopressin (AVP), or its analogue terlipressin, has been proposed as an alternative treatment in the early stages of hypovolemic shock. Design. A meta-analysis of randomized controlled animal trials. Participants. A total of 433 animals from 15 studies were included. Interventions. The ability of AVP and terlipressin to reduce mortality when compared with fluid resuscitation therapy, other vasopressors (norepinephrine or epinephrine), or placebo was investigated. Measurements and Main Results. Pooled estimates showed that AVP and terlipressin consistently and significantly improve survival in hemorrhagic shock (mortality: 26/174 (15%) in the AVP group versus 164/259 (63%) in the control arms; ; 95% CI 0.05 to 0.15; for effect < 0.001; for heterogeneity = 0.30; ). Conclusions. Results suggest that AVP and terlipressin improve survival in the early phases of animal models of hemorrhagic shock. Vasopressin seems to be more effective than all other treatments, including other vasopressor drugs. These results need to be confirmed by human clinical trials.

Cossu, A., Mura, P., De Giudici, L., Puddu, D., Pasin, L., Evangelista, M., Xanthos, T., Musu, M., Finco, G., Vasopressin in hemorrhagic shock: a systematic review and meta-analysis of randomized animal trials, <<BIOMED RESEARCH INTERNATIONAL>>, 2014; Volume 2014 (2014), Article ID 421291, 9 pages (Settembre): N/A-N/A. [doi:http://dx.doi.org/10.1155/2014/421291] [http://hdl.handle.net/10807/64275]

Vasopressin in hemorrhagic shock: a systematic review and meta-analysis of randomized animal trials

Evangelista, Maurizio;
2014

Abstract

Objective. The latest European guidelines for the management of hemorrhagic shock suggest the use of vasopressors (norepinephrine) in order to restore an adequate mean arterial pressure when fluid resuscitation therapy fails to restore blood pressure. The administration of arginine vasopressin (AVP), or its analogue terlipressin, has been proposed as an alternative treatment in the early stages of hypovolemic shock. Design. A meta-analysis of randomized controlled animal trials. Participants. A total of 433 animals from 15 studies were included. Interventions. The ability of AVP and terlipressin to reduce mortality when compared with fluid resuscitation therapy, other vasopressors (norepinephrine or epinephrine), or placebo was investigated. Measurements and Main Results. Pooled estimates showed that AVP and terlipressin consistently and significantly improve survival in hemorrhagic shock (mortality: 26/174 (15%) in the AVP group versus 164/259 (63%) in the control arms; ; 95% CI 0.05 to 0.15; for effect < 0.001; for heterogeneity = 0.30; ). Conclusions. Results suggest that AVP and terlipressin improve survival in the early phases of animal models of hemorrhagic shock. Vasopressin seems to be more effective than all other treatments, including other vasopressor drugs. These results need to be confirmed by human clinical trials.
2014
Inglese
Cossu, A., Mura, P., De Giudici, L., Puddu, D., Pasin, L., Evangelista, M., Xanthos, T., Musu, M., Finco, G., Vasopressin in hemorrhagic shock: a systematic review and meta-analysis of randomized animal trials, <<BIOMED RESEARCH INTERNATIONAL>>, 2014; Volume 2014 (2014), Article ID 421291, 9 pages (Settembre): N/A-N/A. [doi:http://dx.doi.org/10.1155/2014/421291] [http://hdl.handle.net/10807/64275]
File in questo prodotto:
File Dimensione Formato  
421291.pdf

accesso aperto

Descrizione: ARTICOLO PRINCIPALE
Dimensione 1.43 MB
Formato Adobe PDF
1.43 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/64275
Citazioni
  • ???jsp.display-item.citation.pmc??? 11
  • Scopus 35
  • ???jsp.display-item.citation.isi??? 25
social impact