Ac. Krismer et al., The effects of endogenous and exogenous vasopressin during experimental cardiopulmonary resuscitation, ANESTH ANAL, 92(6), 2001, pp. 1499-1504
Citations number
20
Categorie Soggetti
Aneshtesia & Intensive Care","Medical Research Diagnosis & Treatment
Exogenous vasopressin is a promising vasopressor when blood pressure is cri
tically threatened, but the role of endogenous vasopressin during cardiopul
monary resuscitation (CPR) is unknown. We assessed the role of endogenous v
ersus exogenous vasopressin in a porcine open chest CPR model. Seven minute
s before induction of cardiac arrest, seven pigs received 10 mug/kg of a se
lective vasopressin V-1-receptor-antagonist (Blocked Vasopressin group); an
other 12 pigs in two groups received saline administration only. After 4 mi
n of untreated ventricular fibrillation followed by 3 min of basic life sup
port CPR, six animals received 0.8 U/kg vasopressin (Exogenous Vasopressin
group), whereas the blocked vasopressin group (n = 7), and the remaining si
x animals received saline placebo only (Endogenous Vasopressin group). Defi
brillation was attempted after 14 min of CPR. During basic life support CPR
, left ventricular myocardial blood flow was significantly (P < 0.05) decre
ased in the Blocked Vasopressin group compared with the Exogenous Vasopress
in group and Endogenous Vasopressin group (42 +/- 5 compared with 64 +/- 6
and 66 +/- 6 mL . min(-1) 100g(-1)). Left ventricular myocardial blood flow
was significantly decreased in the Blocked Vasopressin group versus Exogen
ous Vasopressin group versus Endogenous Vasopressin group 90 s and 5 min af
ter drug administration, respectively (38 +/- 4 and 27 +/- 3 vs 145 +/- 32
and 110 +/- 12 vs 62 +/- 4 and 56 +/- 6 mL . min(-1) 100g(-1), respectively
). None of seven Blocked Vasopressin animals, six of six Exogenous Vasopres
sin pigs, and six of six Endogenous Vasopressin swine had return of spontan
eous circulation after 14 min of cardiac arrest including 10 min of CPR (P
< 0.05). In conclusion, pigs with blocked endogenous vasopressin had poor c
oronary perfusion pressure and left ventricular myocardial blood flow durin
g open chest CPR, and could not be successfully resuscitated. All pigs with
effective endogenous vasopressin or pigs with effective endogenous vasopre
ssin and additional exogenous vasopressin had good left ventricular myocard
ial blood flow during experimental CPR, and survived the l-h postresuscitat
ion phase. We conclude that endogenous vasopressin is an adjunct vasopresso
r to epinephrine and may serve as a back-up regulator to maintain cardiocir
culatory homeostasis.