Between 1965 and 1995 the incidence of heart failure has been constant
ly rising and the mortality from this disease has increased fivefold.
The introduction of ACE-inhibitors and of adrenergic beta-blockers hav
e resulted in major symptomatic improvements in patients with mild to
moderate heart failure. For end-stage disease, heart transplantation o
ffers by now the only therapeutic option and yields excellent results.
The permanent implantation of left heart assist-devices is just gaini
ng increasing importance. Yet, both methods also have inherent drawbac
ks and may not be available to all patients, so that new methods are c
onstantly evaluated. Cardiomyoplasty was introduced into clinical prac
tice in 1985 by Alain Carpentier and since then more than 700 patients
have been operated worldwide. After dissection of the latissimus dors
i muscle it is wrapped around the heart in a clockwise fashion (Figure
1). Two sensing electrodes are placed on the anterior aspect of the r
ight ventricle and two stimulation electrodes between the proximal bra
nches of the thoracodorsal nerve (Medtronic SP 5548). The electrodes a
re then connected with a burststimulator (Cardiomyostimulator(TM), Med
tronic 4710) (Figure 2). During the first 2 weeks following the operat
ion the muscle is not stimulated in order to allow for the healing pro
cess. Thereafter, a stimulation protocol with a programmed, staged inc
rease of the stimulation frequency is started, to induce transformatio
n of the skeletal muscle into a ''fatigue resistant'' tissue. After 3
months the muscle is stimulated with every second heart beat (2 : 1 mo
de) with full burstimpulses containing 6 single impulses per burst for
a duration of 185 ms (Figure 3). Cardiomyoplasty was conceived for pa
tients in NYHA III and severly impaired myocardial function, in whom d
rug treatment does not produce the expected benefits. The criteria for
patient selection are strictly followed, since it has been shown in t
he past, that the preoperative condition of the patient is of specific
importance for the postoperative outcome. Contraindications are NYHA
IV, advanced right ventricular dysfunction, secundary pulmonary hypert
ension (> 600 dyn x s x cm(-5)), LV end-diastolic diameter > 70 mm und
AV-valve incompetence > Grad II. Between July 1985 und October 1996 6
47 patients received a cardiomyoplasty with the Medtronic Cardiomyopla
sty System and the results from 438 patients were analyzed from the,,W
orldwide Cardiomyoplasty Study Group''. One and 2 years following the
operation NYHA-class had improved by one class in 41,9% and 53,3%, res
pectively, and by 2 classes in 38,1% and 30,5%, respectively. In 16% a
nd 15% no improvement was found (Figure 4). Prospective investigation
of the quality of life by a score revieled a considerable improvement
in the level of daily activities and social interaction. In contrast,
two years after the operation, only a small, but significant increase
in LV-EF from 22,9 +/- 8,1% to 25,8 +/- 9,7% (p < 0,05) was shown. Hea
rt rate, maximal O-2-consumption, total exercise time, cardiac index,
stroke volume and stroke work index did not change. According to the r
esults of a recent FDA-study, in-hospital mortality was 12% between 19
91 and 1993, and was reduced during a second phase starting 1994 to <
3%. One, 2 and 3-year survival of 349 patients who were in NYHA III pr
ior to the operation was 69%, 56% und 47%, respectively. 43 patients w
ho were operated in NYHA IV exhibited considerably worse survival with
only 48% after 1 year and 30% after 2 years, respectively. In a subgr
oup of 103 patients with a statistically low operative risk, 1,2 and 3
-year survival was 77%, 71% und 61%, respectively (Figure 5). As a mec
hanism of action the skeletal muscle wrap exerts some active improveme
nt of systolic wall motion of the heart/skeletal muscle complex. Howev
er, probably more important is an acute and chronically persisting shi
ft of the pressure-volume relation to the left. This process results i
n a ''reverse remodeling'' of the insufficient heart with an improveme
nt of the ''contractility reserve'' (Figure 6).