Key result
Pharmacologic management of acute heart failure relies primarily on beta-adrenoceptor agonists, with phosphodiesterase type III inhibitors serving as an alternative in selected patients.
This review highlights the roles of beta-agonists, PDE III inhibitors, and combination therapies in managing perioperative acute heart failure.
Supports beta-agonists as primary in perioperative acute HF; leaves open optimal PDE III inhibitor selection and combinations.
Because of improved social and medical standards in the western world, the average age of the population continues to increase. This altering demographic profile has its impact on the surgical population, resulting in a dramatic increase in the number of patients with exten sive cardiovascular disease, presenting for either car diac or noncardiac surgery. As a result, the incidence of perioperative acute congestive heart failure (CHF) is a major clinical problem at the present time. For the pharmacologic management of acute CHF, the β-adreno ceptor agonists continue to be the mainstay of therapy, due to their short duration of action and hemodynamic controlability by continuous intravenous infusion. Mono therapy with the phosphodiesterase type III (PDE) inhibi tors appears to be the treatment of choice in selected patients with high systemic vascular resistance or re sidual β-adrenoceptor blockade. Combination therapy especially deserves attention, because this approach allows the enhancement of contractile force, possibly without the side effects associated with the administra tion of high concentrations of one agent alone. New developments including ultrashort-acting PDE inhibi tors, calcium-dependent calcium sensitizers, and cal cium promotors are anxiously awaited.
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Margreeth B. Vroom (1998) conducted a review in Perioperative acute congestive heart failure. Pharmacologic management (beta-adrenoceptor agonists, PDE III inhibitors) was evaluated. Pharmacologic management of acute heart failure relies primarily on beta-adrenoceptor agonists, with phosphodiesterase type III inhibitors serving as an alternative in selected patients.
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