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1 f pump support (bridge to transplantation or destination therapy).
2 eutic intention (bridge to transplant versus destination therapy).
3 ed goal of use (bridge to transplantation or destination therapy).
4 oal of support (bridge to transplantation or destination therapy).
5 ts who are not deemed transplant candidates (destination therapy).
6 52% had ischemic cardiomyopathy and 54% were destination therapy.
7 er LVAD and is associated with older age and destination therapy.
8 as a bridge to cardiac transplantation or as destination therapy.
9 t transplantation, previously referred to as destination therapy.
10 ates in patients receiving these devices for destination therapy.
11 have been used and allow the possibility of destination therapy.
12 te II implantation, with 62% LVADs placed as destination therapy.
13 43% versus 32% of patients had VADs as a destination therapy.
14 bridge to transplant, bridge to recovery or destination therapy.
15 re impairment) seen in patients implanted as destination therapy.
16 nclude use of high-risk transplant lists and destination therapy.
17 e to transplantation, also called chronic or destination therapy.
18 idge to transplantation, may also be used as destination therapy.
19 n in the patients who received the device as destination therapy.
20 ts to provide support until transplant or as destination therapy.
21 ed for the patients who received the pump as destination therapy.
22 respectively, and 61.1% received implants as destination therapy.
23 st be addressed before TAHs can be used as a destination therapy.
24 sed as a bridge to heart transplantation and destination therapy.
25 se as a bridge to lung transplantation or as destination therapy.
26 s are now being used as a permanent form of "destination" therapy.
27 p = 0.001), had MCS more often implanted as destination therapy (33% vs. 14% vs. 22%, p = 0.03), req
29 t devices are also being expanded to include destination therapy and alternatives to cardiac transpla
30 ics encouraged inclusion of all indications (destination therapy and bridge to transplant) and preven
31 end-stage heart disease as either bridge or destination therapy, and have significantly improved the
32 schemic cardiomyopathy, LVAD implantation as destination therapy, and increased baseline body mass in
33 rdiotomy shock, "bridge to transplant," and "destination therapy." At present, device development, cl
34 ional capacity, even among those intended as destination therapy because of ineligibility for transpl
35 , and clinical subgroups of device strategy (destination therapy, bridge to transplant, and bridge to
36 IIB/IV patients meeting indications for LVAD destination therapy but not dependent on intravenous ino
37 ridge to transplantation (BTT) (n = 281) and destination therapy (DT) (n = 374) trials were analyzed.
38 f left ventricular assist devices (LVADs) as destination therapy (DT) can provide survival superior t
40 S) candidates, no matter whether MCS will be destination therapy (DT) or a bridge to heart transplant
46 ability of left ventricular assist device as destination therapy (DT-LVAD) to prolong survival for ma
47 dian age: 62 years, 80% male, 65% White, 61% destination therapy due to transplant ineligibility) was
52 ss associated with continuous-flow LVADs for destination therapy has improved significantly relative
53 splantation and, more recently, as a form of destination therapy has provided a great opportunity to
54 orporation, Pleasanton, California) LVAD for destination therapy has provided an attractive option fo
55 ernative to heart transplantation, so-called Destination Therapy, has become a promising new option f
56 ence interval 1.46-3.44; P(trend)<0.001) and destination therapy (hazard ratio, 1.42; 95% confidence
57 left ventricular assist devices (LVADs) for destination therapy in advanced heart failure and progre
58 are expected to explore compassionate use as destination therapy in carefully selected adult patients
59 pproved for use as a bridge-to-transplant or destination therapy in patients who have irreversible en
60 tance devices are now used increasingly as a destination therapy in patients with advanced heart fail
61 rm support, as a bridge to transplant, or as destination therapy in patients with end-stage systolic
62 , both as a bridge to transplantation and as destination therapy in those who are ineligible for card
66 entification of a dedicated caregiver before destination therapy left ventricular assist device (DT L
69 ge to transplantation and more recently as a destination therapy, left ventricular assist device supp
75 HMII bridge to transplantation (n = 405) and destination therapy (n = 551) clinical trials were retro
78 ntinuous-flow LVADs as bridge to transplant, destination therapy, or bridge to decision from January
79 e, either as a bridge to transplantation, as destination therapy, or in some patients, as a bridge to
81 is study sought to assess the utility of the Destination Therapy Risk Score (DTRS) in patients with c
82 ival Score, Seattle Heart Failure Model, and Destination Therapy Risk Score may provide guidance for
83 rability and complications, the potential of Destination Therapy should continue to expand through th
85 537 LVAD recipients (mean 57+/-13 years, 49% destination therapy, support 18.9 months) prevalence of
86 ailure and the expanded indication use (i.e. destination therapy), the overall number of implanted pa
88 into the HMII bridge to transplantation and destination therapy trials (N = 1,122) were randomly div
90 effectiveness of continuous-flow devices for destination therapy versus optimal medical management in
91 oncerning survival and quality of life since destination therapy was first introduced 10 years ago.
92 e to transplant, bridge to recovery, or even destination therapy will become increasingly important.
93 ear survival rate for patients supported for destination therapy with a continuous-flow LVAD is 74%,