Skip Navigation

European Journal of Heart Failure 2001 3(5):601-610; doi:10.1016/S1388-9842(01)00165-9
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (12)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Capomolla, S.
Right arrow Articles by Cobelli, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Capomolla, S.
Right arrow Articles by Cobelli, F.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 2001 European Society of Cardiology

Chronic infusion of dobutamine and nitroprusside in patients with end-stage heart failure awaiting heart transplantation: safety and clinical outcome

Soccorso Capomollaa,*, Oreste Feboa, Cristina Opasichb, Giampaolo Guazzottia, Angelo Caporotondia, Maria Teresa La Roverea, Marco Gnemmia, Andrea Mortarac, Margherita Vonaa, Gian Domenico Pinnaa, Roberto Maestria and Franco Cobellia

a Fondazione S. Maugeri, Clinica del Lavoro e della Riabilitazione, IRCCS Istituto scientifico di Montescano Pavia, Italy
b Istituto scientifico di Pavia Pavia, Italy
c Policlinico di Monza Milano, Italy

* Corresponding author. Tel.: +39-0385-2471; fax: +39-0385-61386. E-mail address: scapomolla{at}fsm.it (S. Capomolla)


   Abstract

Background: in patients with severe heart failure additional therapeutic support with intravenous inotropic or vasodilator drugs is frequently employed in an attempt to obtain hemodynamic and clinical control. No data comparing the use and efficacy of chronic intravenous inotropic and vasodilator therapy in patients with advanced heart failure are available.

Aims: we evaluated, in a group of patients with advanced heart failure undergoing chronic infusion with dobutamine or nitroprusside, in addition to optimized oral therapy, (1) the safety of chronic infusion, (2) the efficacy of both drugs in managing unloading therapy and (3) clinical outcome of the two therapeutic strategies.

Methods: one hundred and thirteen patients receiving optimized oral therapy, in functional class III/IV with symptoms and signs of refractory heart failure and requiring additional pharmacological support with either intravenous dobutamine or nitroprusside were evaluated. Clinical and therapeutic management and clinical outcome of the two groups were considered.

Results: dobutamine was administered for 12 h/day for 20 ± 23 days at a dosage of 7 ± 3 µg/kg/min to 43 patients. The mean dose of nitroprusside was 0.76 ± 0.99 µg/kg/min. The mean duration of use of this drug, administered as a 12-h/day infusion was 22 ± 38 days. Nitroprusside infusion allowed greater doses of short-term ACE-inhibitors to be used compared to pre-infusion (ACE-inhibitor dose: 55 ± 30 mg/day vs. 127 ± 30 mg/day P < 0.0001) and during dobutamine infusion (ACE-inhibitor dose: 85 ± 47 mg/day vs. 127 ± 30 mg/day P < 0.002). Nitroprusside unlike dobutamine significantly improved the NYHA functional class. Of the 113 patients, 109 (97%) had a cardiac event during a mean follow-up of 337 ± 264 days. Forty-four patients required hospitalization for worsening congestive heart failure, 45/113 (39%) patients died during the follow-up and 27/113 (24%) patients had a heart transplant in status one. Hospitalization, because of worsening heart failure was less frequent in the nitroprusside than in the dobutamine subgroup [29/51 (57%) vs. 19/22 (86%) P < 0.02]. The overall mortality was 28% (20/70) in the nitroprusside group and 58% (25/43) in the dobutamine group (odds ratio 0.33 CI 0.16 to 0.73 P < 0.006). In the group treated with nitroprusside, heart transplantation in status one was performed in 16/33 patients (48%), while in the dobutamine group this was done in 11/14 patients (78%) (odds ratio 0.25 CI 0.06–1.02 P < 0.06). There was a significant reduction in the combined end-point of mortality/heart transplantation in status one in patients treated with nitroprusside compared to those treated with dobutamine (36/70 (51%) vs. 36/43 (84%) — (odds ratio 0.34 CI 0.14–0.80 P < 0.01). The incidence of adverse events in the patients treated with nitroprusside was similar to that in those treated with dobutamine (20% vs. 17% P = ns).

Conclusions: for patients awaiting heart transplantation chronic intermittent nitroprusside infusions are more effective and safer than dobutamine in relieving symptoms, facilitating unloading therapy management and improving survival. Whether chronic intermittent infusion of nitroprusside could represent a feasible medical strategy in out-patients with severe heart failure remains to be investigated.

Key Words: Severe heart failure • Chronic infusion • Nitroprusside • Dobutamine

Received December 15, 2000; Revised February 28, 2001; Accepted April 26, 2001


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
N. Paolocci, T. Katori, H. C. Champion, M. E. St. John, K. M. Miranda, J. M. Fukuto, D. A. Wink, and D. A. Kass
From the Cover: Positive inotropic and lusitropic effects of HNO/NO- in failing hearts: Independence from beta -adrenergic signaling
PNAS, April 29, 2003; 100(9): 5537 - 5542.
[Abstract] [Full Text] [PDF]


Home page
Eur J Heart FailHome page
B. Greenberg, C. Borghi, and S. Perrone
Pharmacotherapeutic approaches for decompensated heart failure: a role for the calcium sensitiser, levosimendan?
Eur J Heart Fail, January 1, 2003; 5(1): 13 - 21.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.