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Transplant of stunned donor hearts rescued by pharmacological stress echocardiography: a “proof of concept” report

  • Tonino Bombardini1Email author,
  • Sonia Gherardi2,
  • Ornella Leone3,
  • Rosa Sicari1 and
  • Eugenio Picano1
Cardiovascular Ultrasound201311:27

https://doi.org/10.1186/1476-7120-11-27

©  Bombardini et al.; licensee BioMed Central Ltd. 2013

Received: 14 July 2013

Accepted: 30 July 2013

Published: 2 August 2013

Open Peer Review reports

Abstract

Background

Due to the shortage of donor hearts, the criteria for acceptance have been considerably expanded. Hearts with regional or global left ventricular dysfunction are excluded from donation, but stress echo might be useful to identify patients with reversible wall motion abnormalities, potentially eligible for donation.

Methods

Six marginal candidate donors (mean age, 40 ± 13 years; three men) were enrolled. Resting echocardiography showed in all subjects a LV ejection fraction ≥ 45% (mean 51 ± 5%), but multiple risk factors were present. All donors had either global or discrete wall motion abnormalities: Wall Motion Score Index (WMSI) rest = 1.33 ± 0.25. Stress echocardiography was performed with the dipyridamole high dose of 0.84 mg/kg given over 6 min.

Results

The stress echo results were abnormal in three donors (WMSI rest = 1.51 ± 0.19 vs peak = 1.41 ± 0.30). These hearts were excluded from donation and cardiac pathology verification was available in two cases of confirmed LV myocardial fibrosis and/or severe coronary stenosis. The remaining three hearts improved during stress (WMSI rest = 1.15 ± 0.13 vs peak = 1.04 ± 0.06) and were transplanted uneventfully. Recipients (three males, mean age 53 ± 4 years) underwent post-TX coronary angiography, IVUS and endomyocardial biopsies. No recipient had primary graft failure, and all showed normal coronary angiography and normal LV function (EF = 57 ± 6%; WMSI = 1 ± 0) at 1-month post-TX. The recipients were alive at 12-month median follow-up.

Conclusions

Dipyridamole stress echo performed in brain-dead potential donors with LV resting global or discrete wall motion abnormalities identifies hearts with severe morphologic abnormalities excluded from donation (with fixed response during stress echo) from hearts eligible for donation, showing improvement in regional wall motion during stress (viability response) and normal function and coronary anatomy following transplantation.

Keywords

Heart transplantHeart donor shortageStress echocardiographyReversible wall motion abnormalitiesEarly graft failure

Background

Brain death is a hostile environment for the donor heart and undoubtedly contributes to the occurrence of primary graft failure after HT. Donor heart dysfunction results from the “catecholamine storm” (hypertension, tachycardia, and intense vasoconstriction) that produces an increase in myocardial oxygen demand and potentially myocardial ischemia. These phenomena may mediate myofibrillar degeneration, a process characterized by injury and death of myofibers in a hypercontracted state [1]. Myocardial injury interacts with other factors, increasing the probability of post-operative primary graft dysfunction [2]. Donor risk factors known to be associated with early graft failure include higher doses of inotropic support and longer ischemic time, depressed systolic function (especially discreet wall motion abnormalities), and older donor age [3].

As far as function is concerned, a donor heart should not be used in the presence of intractable ventricular arrhythmias, the need for excessive inotropic support, discreet wall motion abnormalities on echocardiography or LVEF < 45% despite optimization of hemodynamics with inotropic support [2]. Given that a single echocardiographic assessment may be inaccurate or may fail to predict long-term ventricular contractile function, failure to use a donor heart because of the initial ejection fraction alone is not justified. Hemodynamic and metabolic management should be performed before the organ is declined, when donor left ventricular dysfunction is present [4, 5]. Recent studies have shown that pharmacological stress echo is feasible for recruiting older donor hearts that were excluded simply because of the age limit in patients with normal resting function [6, 7]. Pharmacological stress echo might be a feasible technique in intensive care units, to distinguish between hearts with reversible (eligible for transplant) vs non-reversible left ventricular segmental wall motion abnormalities. A practical advantage is the 2011 Italian National Institute of Health approval of echo stress methodology for heart donor selection in Italy with a second-opinion telemedicine system from the core echo lab, IFC, Pisa [8].

Aim of this study was to evaluate the usefulness of dipyridamole stress echocardiography in selecting for heart TX hearts with “standard” donor age but with multiple risk factors for early graft failure and discreet LV wall motion abnormalities in resting echocardiogram. The study hypothesis was that hearts with fixed abnormalities were not eligible as proven at cardio-autoptic verification, whereas those with reversible abnormalities were potentially eligible for transplantation as shown by subsequent angiographic evaluation in transplanted hearts.

Methods

Marginal donor recruitment

After legal declaration of brain death, marginal donors underwent baseline echocardiography for evaluation of regional wall motion, global ventricular function, and ventricular mass, according to American Society of Echocardiography recommendations [9].

Donor selection by stress echocardiographic criteria

Stress echocardiography was performed following the European Association of Echocardiography and American Society of Echocardiography [10, 11] protocol, using dipyridamole (0.84 mg/kg over 6 min). Echocardiographic images were continuously recorded and intermittently digitized. Regional wall motion score index was assessed and graded on a scale from 1 (normal) to 4 (dyskinetic) in each of the 17 segments at rest and after stress. LV wall motion score index was calculated by summing the scores and dividing the sum by 17. By definition, donors with abnormal stress echocardiographic results had fixed wall motion abnormalities and/or stress-induced wall motion abnormalities. We also considered changes in LV volumes as an index of global dysfunction, and pressure and volume changes as an index of LV elastance [6, 12]. At baseline and peak stress, the projections of the four chambers and of the two apical chambers were recorded to obtain LV end-systolic volume using the biplane Simpson rule [9] to calculate LV elastance (the ratio of systolic pressure by cuff sphygmomanometry to LV end-systolic volume) [12]. A decrease in LV elastance during stress was considered abnormal. In a previous study, this response was shown to be associated with moderate to severe coronary or myocardial abnormalities on cardiac autopsy verification [13]. Potential donors with normal stress echocardiography are considered suitable donors; recipients follow a routine treatment. We accepted a priori four stress echocardiographic criteria excluding a heart from eligibility as a donor: (1) new regional wall motion abnormalities (regional wall motion score > 1.0 in at least one segment), (2) abnormal regional or global LV dysfunction with fixed response to stress; (3) negative LV elastance variation during stress (stress value less than resting value), and (4) submaximal stress prematurely stopped because of non-diagnostic limiting effects (e.g., hemodynamic instability or hypotension with a decrease > 40 mmHg in systolic or diastolic blood pressure) before completion of the infusion. Each of the four criteria had a different rationale and target: a new-onset regional wall motion abnormality is a highly specific sign of a significant epicardial artery stenosis [10, 11]; a fixed response of abnormal regional or global LV function is a specific sign of an irreversibly damaged heart that will not recover, due to extensive necrosis or scarring, and is not eligible for transplant; a lack of hyperkinetic response with no increase in pressure/volume index is a sensitive marker of underlying cardiomyopathy [6], and a submaximal test loses diagnostic and prognostic power and falls within a gray zone unacceptable in the transplantation setting [10, 11]. Eligible organs were considered for transplantation [14]. Hearts that were not eligible underwent pathologic examination [13].

Transplantation of eligible hearts

Eligible hearts (with normal echocardiographic findings) were retrieved using a standard technique and preserved with cold cardioplegic arrest and topical hypothermia. Primary graft failure after HT was defined as need for immediate post-HT mechanical circulatory support [3]. The recipients followed routine treatment and follow-up procedures. They underwent coronary angiography and intravascular ultrasound at the first month [3]. Focal and non-circumferential atherosclerosis with 50% stenosis in proximal segments of at least one coronary vessel was regarded as native and donor-transmitted coronary atherosclerosis [15]. Endomyocardial biopsies (EMBs) were taken for post-transplant rejection status surveillance. All transplanted hearts were followed, and any adverse event was monitored.

Anatomic-pathologic study of non-transplanted hearts

Hearts deemed unsuitable as a result of stress echocardiographic results were removed from donors and sent to the Pathology Department Center for a very detailed macroscopic and microscopic study [13]. Autopsies were performed by an experienced cardiac pathologist. Coronary atherosclerosis was graded as absent, subcritical, or significant. In accordance with the criteria of cardiac catheterization given above, significant atherosclerosis was defined as focal and non-circumferential atherosclerosis with 50% stenosis in proximal segments of at least one coronary vessel.

Statistical analysis

SPSS version 11 for Windows (SPSS, Inc., Chicago, IL, USA) was used for statistical analyses. The statistical analyses included descriptive statistics (frequencies and percentages for categorical variables and mean ± standard deviation for continuous variables). P values < .05 were considered statistically significant.

Results

Six marginal candidate donors (mean age, 40 ± 13 years; three men) were enrolled (Table 1). The causes of death were head trauma in two, cerebral vascular accident in three, and cardiac arrest in one. Resting echocardiography showed in all a LVEF ≥ 45%, mean value = 51 ± 5%, but multiple risk factors were present: all were heavy smokers, three had elevated cardiac markers, three had central venous pressure > 12 mmHg, three had need for excessive inotropic support, all six had either global or discrete wall motion abnormalities, with WMSI at rest = 1.33 ± 0.25. Stress echocardiography was performed with high-dose dipyridamole (0.84 mg/kg over 6 min).
Table 1

Donor hearts rescued by stress echocardiography

Donor

#1

#2

#3

#4

#5

#6

Age (years)

53

32

50

20

45

36

Sex

Female

Female

Female

Male

Male

Male

Medical history

      

Brain death cause

Intra-axial hemorrhage

Head injury

Subarachnoid hemorrhage

Cardiac arrest (37 min)

Head injury

Subarachnoid hemorrhage

Smoking

Yes

Yes

Yes

Yes

Yes

Yes

Intensive Care Unit data

      

Troponin T (μg/L)

0.1

0.01

0.01

15*

152*

1073*

Central Venous Pressure (mmHg)

16*

-

7

-

13*

15*

Length of stay before death (days)

5

1

1

-

2

3

Noradrenaline (μg/kg/min)

0.6* Dopamine 10

0.28*

0.02

0.1

-

0.14* + dobutamine 2.8

RESTING Echo

Apical Hypokinesia*

Anterior-septal Hypokinesia*

Apical Akinesia*

Mild LVEF reduction*

Septal Hypokinesia*

Lateral inferior Hypokinesia*

LVEF, rest (%)

51*

46*

55

49*

60

47*

LV mass index (g/m2)

145*

89

112*

89

133*

102

WMSI, rest

1.29*

1.59*

1.65*

1

1.18*

1.26*

Stress echo

      

Dipyridamole infusion (min)

6

6

4*

6

6

6

LVEF, peak (%)

60

56

59

60

75

55

WMSI, peak

1.12*

1.41*

1.71*

1

1

1.11*

Δ WMSI

- 0.17

- 0.18

+ 0.06*

0

- 0.18

- 0.15

ΔESP/ESVi (mmHg/mL/m2)

Negative* (- 0.21)

Flat* (0.08)

Negative* (-1.7)

Positive (+0.94)

Positive (+1.2)

Flat (0)

Autopsy findings

Mild DCM*

-

CAD, 90% LAD coronary stenosis*

-

-

-

Histology

Replacing interstitial fibrosis

-

Coagulative necrosis, colliquative myocytolysis

-

-

-

Heart TX

-

-

-

YES

YES

YES

Cold ischemia time (min)

   

180

172

150

Recipient

      

Age/sex

   

56/M

48/M

55/M

Disease

   

Ischemic DC

Congenital HD

HCM

UNOS Status

   

2

2

2

Post-TX angiography

   

Normal

Normal

Normal

Intravascular Ultrasound-intimal thickness

   

-

LAD focal

0.6 mm LAD

Month 1 LVEF (%)

   

50

62

58

Post TX endomyocardial biopsies

   

regular myocardium

isolated foci of ischemic per transplant injury

regular myocardium

Follow-up months

   

26 alive

9 alive

12 alive

*Not Normal.

Abnormal stress echo response with fixed or worsening wall motion

The stress echo results were abnormal in three donors: WMSI peak = 1.41 ± 0.30, with a flat-negative contractile reserve (Figures 1 and 2) (Additional files 1 and 2). At autopsy study (available in two), the donor with incomplete recovery of apical hypokinesia showed myocardial fibrosis with a mild DCM aspect (Table 1, donor #1); the donor with worsening of apical akinesia (Table 1, donor #3) showed a 90% LAD stenosis, multiple foci of coagulative necrosis associated with diffuse coagulative subendocardial myocytolysis (Figure 3).
Figure 1
Figure 1

Donor #2 in Table  1 . An example of a stress echocardiogram in a brain-dead potential donor, showing end-diastolic and end-systolic frames at rest and following stress using Dipyridamole (0.84 mg/kg in 6’) [see Additional file 1]. Left ventricular interventricular septum and apical wall a-kinesia are shown in parasternal long-axis (panel A) and short-axis (panel B) chamber views. At peak stress an incomplete viability response is shown. The donor was considered unsuitable for heart donation.

Figure 2
Figure 2

Donor #3 in Table  1 . An example of a stress echocardiogram with fixed abnormalities in a brain-dead potential donor, showing end-diastolic and end-systolic frames at rest and following stress using Dipyridamole. The test was prematurely stopped at 4 min due to severe systemic hypotension; WMSI rest = 1.65; WMSI = 1.71 at stop stress [see Additional file 2]. The pressure volume relation was negative with the ΔESP/ESV value = - 1.7 mmHg/mL/m2. The heart was sent to the pathology department for detailed macroscopic and histology examination.

Figure 3
Figure 3

The donor heart unsuitable for transplant of Figure  2 . A) Macroscopic aspect of donor heart. B) Fibro-lipidic plaque narrowing (≈90%) the lumen of left anterior coronary artery (Mallory trichrome stain; original magnification 25x); in the inset, the corresponding macroscopic sample. C) Focus of myocardial coagulative necrosis (arrow) in the left ventricle (Hematoxylin-Eosin stain; original magnification 200x). D) Subendocardial coagulative myocytolysis (arrow) in the septal myocardium (Hematoxylin-Eosin stain; original magnification: 400x).

Additional files 2: LV apical wall akinesia is shown at baseline (left upper panel) and 1-min stress (right upper panel). At 3- and 4-min stress (lower panels) a worsening of LV function is shown accompanied by hemodynamic instability. (AVI 5 MB)

Normal stress echo response with improvement in wall motion

The remaining three hearts showed reversible left ventricular resting abnormalities (Figures 4, 5, 6 and 7) (Additional files 3, 4 and 5). WMSI rest = 1.15 ± 0.13 vs peak = 1.04 ± 0.06. All had positive contractile reserve, with LV elastance increase during stress. These three hearts were transplanted uneventfully and underwent standard post TX coronary, angiography, IVUS and endomyocardial biopsies. The recipients were male, age 53 ± 4 years. No recipient had primary graft failure and all showed normal coronary vessel at 1-month post-TX coronary angiography: left ventricular function was normal at 1 month post-TX (LVEF = 57 ± 6%; WMSI = 1 ± 0). In the EMBs taken for post-transplant rejection status surveillance, no significant ischemic peritransplant injury was noted in two recipients (Table 1, donors #4 and #6) (Figure 6). The recipient of the donor heart with mild left ventricular hypertrophy and reversible septal hypokinesia (Table 1, donor #5) showed at EMBs mild peritransplant injury (Figure 8). The recipients were alive at 12-month median follow-up.
Figure 4
Figure 4

Donor #6 of Table  1 . Two-dimensional transesophageal echocardiogram recorded immediately after “explosive” subarachnoid hemorrhage accompanied by extreme systolic hypertensive response with systolic blood pressure ≈ 300 mmHg and acute pulmonary edema. The donor had discrete left ventricular dysfunction with hypokinesia involving the inferior and lateral LV walls [see Additional file 3].

Figure 5
Figure 5

Donor #6 of Table  1 . The same donor as in Figure 4. Two days after the subarachnoid hemorrhage and after brain death, the donor underwent a transthoracic dipyridamole stress echo (0.84 mg/kg in 6’) [see Additional file 4]. Left ventricular lateral wall hypokinesia and inferior wall akinesia are shown in 4-chamber (panel A) and 3-chamber (panel B) views at baseline (left panels). At peak stress a viability response is shown with recovery of lateral and inferior wall motion (right panels). The donor was considered suitable for heart donation and the heart was transplanted.

Figure 6
Figure 6

The donor heart of donor #6 (Table  1 ) after heart transplant. In the figure, images from the first two endomyocardial biopsies (EMBs) performed on the 7th (panel A) and 15th (panel B) days after surgery, where regular myocardium is shown. In the EMBs taken for post-transplant rejection status surveillance, no significant ischemic peritransplant injury was noted, a finding usually seen in biopsies during the first 6 weeks after transplantation.

Figure 7
Figure 7

Donor #4 of Table  1 . Transthoracic pharmacological stress echo test using dipyridamole (0.84 mg/kg in 6’) in a potential donor with prolonged (37 min) cardiac arrest at death [see Additional file 5]. The donor had normal response with normal regional wall motion during pharmacological stress echo. (panel A, 4-chamber views; panel B, 2-chamber views). The pressure/volume relation was positive and the individual was considered a suitable donor.

Figure 8
Figure 8

Recipient of donor #5 in Table 1 . Ischemic peritransplant injury in the first 4 endomyocardial biopsies (EMBs) taken for post-transplant rejection status surveillance. A (12th day after surgery): generic interstitial oedema; B (19th day after surgery): a focus of peritransplant injury with hypereosinophilic cytoplasm myocites (asterisk) or with coagulative myocytolisis (arrow); C (26th day after surgery): necrotic, evanescent (disappearing) and fragmented myocytes (asterisk); D (36th day after surgery): a focus of resolving peritransplant injury with regional loss of myocytes, loose substitutive connective tissue/granulation tissue and pigment-laden macrophages.

Additional files 5: Quad screen DIP stress echo: global and regional wall motion is shown in 4- and 2-chamber views at baseline (upper panels) and at peak stress (lower panels).(AVI 5 MB)

Discussion

Heart transplantation is an established procedure in end-stage heart failure patients and results in satisfying long-term results. However, this surgical therapy has been limited by a severe and incremental donor organ shortage in the last few years. Therefore, adequate and optimal utilization of all suitable donor organs is mandatory for increasing graft availability. Evidence exists that certain ‘standard’ donor criteria can be significantly liberalized to increase the available donor pool by accepting ‘Marginal Donors’ who would be declined as potential organ donors under conventional transplant guidelines. If echocardiography is the initial assessment investigation, echocardiographically detected left ventricular systolic dysfunction in the absence of a history of heart disease is the single most common cause for non-transplantation of an organ [16]. However, ventricular dysfunction may be transient [17], and arbitrary thresholds of LV function may exclude hearts that could be resuscitated to transplantable status. Recent studies have shown that pharmacological stress echo (with dipyridamole or dobutamine) is a feasible tool for recruiting older donor hearts for transplant, excluded on the basis of age. The ability of pharmacologic stress testing to select these aged donors has been documented by the pathological findings in refused hearts [13] and by the clinical, angiographic and prognostic data in successfully transplanted hearts [6]. The exclusion criterion based on the presence of wall motion abnormalities is potentially overcome by the application of stress echocardiography that may transiently reverse regional dysfunction and identify the subset with a likelihood to recover over time. Such an approach has been widely demonstrated in large multicenter studies showing that the transient improvement induced by either a vasodilator or inotropic response was translated into a stable recovery and a better outcome in stunned or hibernated hearts [11, 18, 19]. In a large subset of brain-dead donor hearts, left ventricular performance is reduced because the myocardium is regionally stunned or hibernating rather than irreversibly infarcted or fibrotic. The detection of reversible dysfunctional myocardium is clinically relevant, as regional or global left ventricular function will improve after transplant. The phenomenon of troponin elevation and cardiac dysfunction in the donor may be transient, suggesting altered sarcolemmal integrity rather than myocyte necrosis [5].

With pharmacological stress, the principle (i.e., the underlying physiological marker) of the test relies on the demonstration of residual contractile reserve in a basally dysfunctional region; improved myocardial thickening of segments that are dyssynergic in resting conditions is a sign of viability, whereas necrotic segments show no functional improvement. Such reserve can be elicited through a flow-mediated increase in contractile function linked to endogenous adenosine accumulation achieved by intravenous infusion of dipyridamole.

Comparison with previous studies

Left ventricular dysfunction is a common finding in patients with intracranial pathologies and brain stem death. In 147 patients with subarachnoid hemorrhage, global or regional LV dysfunction was found in 30 (20%) patients on echocardiography. Regional wall motion abnormalities tended to cover multiple arterial territories and occurred in the absence of coronary artery disease [20]. This frequency has been confirmed in a retrospective study of 66 patients with brain stem death, 28 (42%) of whom were found to have global or segmental LV dysfunction that was not predicted by clinical and electrocardiographic examination [21]. Secondly, left ventricular dysfunction documented on echocardiography in heart donors with BSD does not appear to correspond to any demonstrable pathological abnormality at postmortem [22]. Thirdly, there is clear evidence not only that donor hearts with mild abnormalities in LV function on rest echocardiography can be successfully transplanted but also that donor hearts with more severe regional wall abnormalities may improve immediately post-transplant [23]. The stress echo approach might also be applied to these potential heart donors with left ventricular wall motion abnormalities, since viability response during stress echo effectively recognizes viable tissue with non-fixed response, as opposed to necrotic response with scar and fixed wall motion abnormalities following inotropic challenge with either dobutamine or dipyridamole [24, 25].

Conclusion

Left ventricular dysfunction is common in donor hearts and in several cases does not correspond to a detectable pathological abnormality. Abnormal regional or global resting LV dysfunction is a functionally heterogeneous entity, encompassing patients both unsuitable and suitable for donation. The former group shows fixed or worsening (abnormal) wall motion response during stress echo, and significant myocardial and/or coronary alterations at pathology verification. The second group shows normal (reversible, viability) wall motion response during stress echo, and absence of myocardial and/or coronary alterations at angiography verification, and can be transplanted uneventfully. The promising data obtained in this proof-of-concept study should now be substantiated in a larger series in order to change current guidelines ruling out donation on the basis of probably too-restrictive criteria of global or discreet regional wall motion abnormalities.

Authors’ information

TB, Scientific Coordinator of the CCM project n. 48 “Aged Donor Heart Rescue by Stress Echo – ADONHERS” Institute of Clinical Physiology, National Research Council, Pisa, Italy. SG, Cardiology Division and Intensive Care Unit, M. Bufalini Hospital, Cesena, Italy. OL, Pathology Department, University of Bologna, Italy. RS, is the Head of the Echocardiography Lab, IFC, CNR, Pisa. EP, Director IFC, CNR, Pisa, Italy.

Abbreviations

BSD: 

Brain stem death

DIP: 

Dipyridamole

EF: 

Ejection fraction

EMBs: 

Endomyocardial biopsies

HT: 

Heart transplant

IVUS: 

Intra Vascular ultra sound

LV: 

Left Ventricular

TX: 

Transplant

WMSI: 

Wall motion score index.

Declarations

Acknowledgments

Partial funding for the Stress Echo project was provided by the Italian Health Ministry. (CCM project #48, 2010). Italian National Transplant Center, May 11, 2011 Guidelines: increase available organs for heart transplant with heart assessed by stress echocardiography in older donors or in donors with several risk factors.

We thank Alison Frank for her invaluable work in editing the manuscript.

Authors’ Affiliations

(1)
CNR, Institute of Clinical Physiology, Pisa, Italy
(2)
Cardiology Division, M. Bufalini Hospital, Cesena, Italy
(3)
Department of Pathology, University of Bologna, Bologna, Italy

References

  1. Nguyen H, Zaroff JG: Neurogenic stunned myocardium. Curr Neurol Neurosci Rep. 2009, 6: 486-491.View ArticleGoogle Scholar
  2. Costanzo MR, Dipchand A, Starling R, Anderson A, Chan M, Desai S, Fedson S, Fisher P, Gonzales-Stawinski G, Martinelli L, McGiffin D, Smith J, Taylor D, Meiser B, Webber S, Baran D, Carboni M, Dengler T, Feldman D, Frigerio M, Kfoury A, Kim D, Kobashigawa J, Shullo M, Stehlik J, Teuteberg J, Uber P, Zuckermann A, Hunt S, Burch M: International Society of Heart and Lung Transplantation Guidelines: the International Society for Heart and Lung Transplantation Guidelines for the care of heart transplant recipients. J Heart Lung Transplant. 2010, 29 (8): 914-956. 10.1016/j.healun.2010.05.034.View ArticlePubMedGoogle Scholar
  3. Lietz K, John R, Mancini DM, Edwards NM: Outcomes in cardiac transplant recipients using allografts from older donors versus mortality on the transplant waiting list; implications for donor selection criteria. J Am Coll Cardiol. 2004, 43 (9): 1553-1561. 10.1016/j.jacc.2004.02.002.View ArticlePubMedGoogle Scholar
  4. Zaroff JG, Rosengard BR, Armstrong WF, Babcock WD, D'Alessandro A, Dec GW, Edwards NM, Higgins RS, Jeevanandum V, Kauffman M, Kirklin JK, Large SR, Marelli D, Peterson TS, Ring WS, Robbins RC, Russell SD, Taylor DO, Van Bakel A, Wallwork J, Young JB: Consensus conference report: maximizing use of organs received from cadaver donor-cardiac recommendations, March 28-29, 2001, Crystal City, VA. Circulation. 2002, 106 (7): 836-841. 10.1161/01.CIR.0000025587.40373.75.View ArticlePubMedGoogle Scholar
  5. Dronavalli VB, Banner NR, Bonser RS: Assessment of the potential heart donor: a role for biomarkers?. J Am Coll Cardiol. 2010, 56 (5): 352-361. 10.1016/j.jacc.2010.02.055.View ArticlePubMedGoogle Scholar
  6. Bombardini T, Gherardi S, Arpesella G, Maccherini M, Serra W, Magnani G, Del Bene R, Picano E: Favorable short-term outcome of transplanted hearts selected from marginal donors by pharmacological stress echocardiography. J Am Soc Echocardiogr. 2011, 24 (4): 353-362. 10.1016/j.echo.2010.11.014.View ArticlePubMedGoogle Scholar
  7. Fine NM, Pellikka PA: Pharmacologic stress echocardiography for the assessment of organ suitability for heart transplantation: casting a broader net in search of donors. J Am Soc Echocardiogr. 2011, 24 (4): 363-366. 10.1016/j.echo.2011.02.006.View ArticlePubMedGoogle Scholar
  8. Franchi D, Cini D, Arpesella G, Gherardi S, Calamai I, Barletta G, Valente S, Pasanisi E, Sansoni S, Ricci C, Serra W, Picano E, Bombardini T: Second-opinion stress tele-echocardiography for the Adonhers (Aged donor heart rescue by stress echo) project. Cardiovasc Ultrasound. 2010, 8: 20-10.1186/1476-7120-8-20.View ArticlePubMedPubMed CentralGoogle Scholar
  9. Gardin JM, Adams DB, Douglas PS, Feigenbaum H, Forst DH, Fraser AG, Grayburn PA, Katz AS, Keller AM, Kerber RE, Khandheria BK, Klein AL, Lang RM, Pierard LA, Quinones MA, Schnittger I: American Society of Echocardiography. Recommendations for a standardized report for adult transthoracic echocardiography: a report from the American Society of Echocardiography's Nomenclature and Standards Committee and Task Force for a Standardized Echocardiography Report. J Am Soc Echocardiogr. 2002, 15 (3): 275-290. 10.1067/mje.2002.121536.View ArticlePubMedGoogle Scholar
  10. Pellikka PA, Nagueh SF, Elhendy AA, Kuehl CA, Sawada SG: American Society of Echocardiography recommendations for performance, interpretation, and application of stress echocardiography. J Am Soc Echocardiogr. 2007, 20 (9): 1021-1041. 10.1016/j.echo.2007.07.003.View ArticlePubMedGoogle Scholar
  11. Sicari R, Nihoyannopoulos P, Evangelista A, Kasprzak J, Lancellotti P, Poldermans D, Voigt JU, Zamorano JL: European Association of Echocardiography. Stress Echocardiography Expert Consensus Statement--Executive Summary: European Association of Echocardiography (EAE) (a registered branch of the ESC). Eur Heart J. 2009, 30 (3): 278-289.View ArticlePubMedGoogle Scholar
  12. Bombardini T, Galderisi M, Agricola E, Coppola V, Mottola G, Picano E: Negative stress echo: further prognostic stratification with assessment of pressure-volume relation. Int J Cardiol. 2008, 126 (2): 258-267. 10.1016/j.ijcard.2006.12.093.View ArticlePubMedGoogle Scholar
  13. Leone O, Gherardi S, Targa L, Pasanisi E, Mikus P, Tanganelli P, Maccherini M, Arpesella G, Picano E, Bombardini T: Stress echocardiography as a gatekeeper to donation in aged marginal donor hearts: anatomic and pathologic correlations of abnormal stress echocardiography results. J Heart Lung Transplant. 2009, 28 (11): 1141-1149. 10.1016/j.healun.2009.05.029.View ArticlePubMedGoogle Scholar
  14. Cullen MW, Pellikka PA: Recent advances in stress echocardiography. Curr Opin Cardiol. 2011, 26 (5): 379-384. 10.1097/HCO.0b013e328349035b.View ArticlePubMedGoogle Scholar
  15. Grauhan O, Patzurek J, Hummel M, Lehmkuhl H, Dandel M, Pasic M, Weng Y, Hetzer R: Donor-transmitted coronary atherosclerosis. J Heart Lung Transplant. 2003, 22 (5): 568-573. 10.1016/S1053-2498(02)00655-1.View ArticlePubMedGoogle Scholar
  16. Hertz MI, Aurora P, Christie JD, Dobbels F, Edwards LB, Kirk R, Kucheryavaya AY, Rahmel AO, Rowe AW, Stehlik J, Taylor DO: Scientific Registry of the International Society for Heart and Lung Transplantation: introduction to the 2009 Annual Reports. J Heart Lung Transplant. 2009, 28 (10): 989-992. 10.1016/j.healun.2009.08.005.View ArticlePubMedGoogle Scholar
  17. Zaroff JG, Babcock WD, Shiboski SC, Solinger LL, Rosengard BR: Temporal changes in left ventricular systolic function in heart donors: results of serial echocardiography. J Heart Lung Transplant. 2003, 22 (4): 383-388. 10.1016/S1053-2498(02)00561-2.View ArticlePubMedGoogle Scholar
  18. Piérard LA, De Landsheere CM, Berthe C, Rigo P, Kulbertus HE: Identification of viable myocardium by echocardiography during dobutamine infusion in patients with myocardial infarction after thrombolytic therapy: comparison with positron emission tomography. J Am Coll Cardiol. 1990, 15 (5): 1021-1031. 10.1016/0735-1097(90)90236-I.View ArticlePubMedGoogle Scholar
  19. Picano E: Stress echocardiography. From pathophysiological toy to diagnostic tool. Circulation. 1992, 85 (4): 1604-1612. 10.1161/01.CIR.85.4.1604.View ArticlePubMedGoogle Scholar
  20. Zaroff JG, Rordorf GA, Ogilvy CS, Picard MH: Regional patterns of left ventricular systolic dysfunction after subarachnoid hemorrhage: evidence for neurally mediated cardiac injury. J Am Soc Echocardiogr. 2000, 13 (8): 774-779. 10.1067/mje.2000.105763.View ArticlePubMedGoogle Scholar
  21. Venkateswaran RV, Bonser RS, Steeds RP: The echocardiographic assessment of donor heart function prior to cardiac transplantation. Eur J Echocardiogr. 2005, 6 (4): 260-263. 10.1016/j.euje.2004.10.008.View ArticlePubMedGoogle Scholar
  22. Dujardin KS, McCully RB, Wijdicks EF, Tazelaar HD, Seward JB, McGregor CG, Olson LJ: Myocardial dysfunction associated with brain death: clinical, echocardiographic, and pathologic features. J Heart Lung Transplant. 2001, 20 (3): 350-357. 10.1016/S1053-2498(00)00193-5.View ArticlePubMedGoogle Scholar
  23. Seiler C, Laske A, Gallino A, Turina M, Jenni R: Echocardiographic evaluation of left ventricular wall motion before and after heart transplantation. J Heart Lung Transplant. 1992, 11 (5): 867-874.PubMedGoogle Scholar
  24. Kono T, Nishina T, Morita H, Hirota Y, Kawamura K, Fujiwara A: Usefulness of low-dose dobutamine stress echocardiography for evaluating reversibility of brain death-induced myocardial dysfunction. Am J Cardiol. 1999, 84 (5): 578-582. 10.1016/S0002-9149(99)00382-3.View ArticlePubMedGoogle Scholar
  25. Leone O, Veinot JP, Angelini A, Baandrup UT, Basso C, Berry G, Bruneval P, Burke M, Butany J, Calabrese F, D’Amati G, Edwards WD, Fallon JT, Fishbein MC, Gallagher PJ, Halushka MK, McManus B, Pucci A, Rodriguez ER, Saffitz JE, Sheppard MN, Steenbergen C, Stone JR, Tan C, Thiene G, van der Wal AC, Winters GL: 2011 consensus statement on endomyocardial biopsy from the Association for European Cardiovascular Pathology and the Society for Cardiovascular Pathology. Cardiovasc Pathol. 2012, 21 (4): 245-274. 10.1016/j.carpath.2011.10.001.View ArticlePubMedGoogle Scholar

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© Bombardini et al.; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Cardiovascular Ultrasound

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