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https://doi.org/10.15836/ccar2024.424

Simultaneous heart-liver and heart-kidney transplantation: a case series from the University Hospital Centre Zagreb

Antun Zvonimir Kovač orcid id orcid.org/0000-0001-6276-4450 ; University Hospital Centre Zagreb, Zagreb, Croatia
Ivo Planinc orcid id orcid.org/0000-0003-0561-6704 ; University Hospital Centre Zagreb, Zagreb, Croatia
Boško Skorić orcid id orcid.org/0000-0001-5979-2346 ; University Hospital Centre Zagreb, Zagreb, Croatia
Nina Jakuš orcid id orcid.org/0000-0001-7304-1127 ; University Hospital Centre Zagreb, Zagreb, Croatia
Dora Fabijanović orcid id orcid.org/0000-0003-2633-3439 ; University Hospital Centre Zagreb, Zagreb, Croatia
Anna Mrzljak orcid id orcid.org/0000-0001-6270-2305 ; University Hospital Centre Zagreb, Zagreb, Croatia
Nikolina Bašić-Jukić orcid id orcid.org/0000-0002-0221-2758 ; University Hospital Centre Zagreb, Zagreb, Croatia
Hrvoje Gašparović orcid id orcid.org/0000-0002-2492-3702 ; University Hospital Centre Zagreb, Zagreb, Croatia
Ante Lekić ; University Hospital Centre Zagreb, Zagreb, Croatia
Željko Čolak orcid id orcid.org/0000-0003-0507-4714 ; University Hospital Centre Zagreb, Zagreb, Croatia
Hrvoje Silovski orcid id orcid.org/0000-0001-7884-8923 ; University Hospital Centre Zagreb, Zagreb, Croatia
Igor Petrović orcid id orcid.org/0000-0002-9642-3774 ; University Hospital Centre Zagreb, Zagreb, Croatia
Ognjan Deban orcid id orcid.org/0009-0002-3906-3300 ; University Hospital Centre Zagreb, Zagreb, Croatia
Željko Kaštelan orcid id orcid.org/0000-0002-9262-3234 ; University Hospital Centre Zagreb, Zagreb, Croatia
Maja Čikeš orcid id orcid.org/0000-0002-4772-5549 ; University Hospital Centre Zagreb, Zagreb, Croatia
Davor Miličić orcid id orcid.org/0000-0001-9101-1570 ; University Hospital Centre Zagreb, Zagreb, Croatia


Puni tekst: engleski pdf 183 Kb

str. 424-425

preuzimanja: 106

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Sažetak

Ključne riječi

heart-liver transplantation; heart-kidney transplantation; ischemic heart disease; hereditary amyloidosis; polycystic kidney disease

Hrčak ID:

327915

URI

https://hrcak.srce.hr/327915

Datum izdavanja:

13.12.2024.

Posjeta: 304 *



Introduction: Dual organ transplantation, such as heart-liver or heart-kidney, is a rare but essential option for patients with multi-organ failure. While outcomes for single-organ transplants are well-documented, reports of dual transplants are limited. (1-3) This case series presents two heart-liver and one heart-kidney transplant cases to provide insights into clinical outcomes and management. Aim: To analyze the clinical characteristics, clinical course, perioperative management, and post-transplant outcomes of patients undergoing simultaneous heart-liver and heart-kidney transplantation at the University Hospital Centre (UHC) Zagreb, Croatia.

Case series: Three patients underwent dual organ transplantation between January 2023 and September 2024. Two patients received heart-liver transplants for heart failure due to hereditary transthyretin amyloidosis, while one patient underwent heart-kidney transplantation for end-stage heart failure secondary to ischemic heart disease and renal failure associated with polycystic kidney disease. Surgical techniques and postoperative care were tailored to each patient’s clinical profile. The first patient, a 49-year-old male who underwent heart-liver transplantation, has a 20-month follow-up. His course included early liver graft rejection, successfully treated with pulse corticosteroids. Heart function remains preserved, and he initially had transient, low-intensity donor-specific antibodies (DSAs). The second patient, a 52-year-old male with heart-liver transplantation, has a one -month follow-up with preserved organ function, no rejection, and no DSAs. The third patient, a 54-year-old male who underwent heart-kidney transplantation, has a one-month follow-up complicated by prolonged postoperative peritoneal drainage, but both grafts are functioning well, with no rejection or DSAs (Table 1).

TABLE 1 Patient characteristics in dual-organ transplantation.
Patient characteristicsCASE 1CASE 2CASE 3
Age, sex49, male52, male54, male
Follow up20 months1 month1 month
Transplanted organsHeart and liverHeart and liverHeart and kidney
Etiology of primary organ failureHereditary TTR amyloidosisHereditary TTR amyloidosisIschemic heart disease
Polycystic kidney disease
Pretransplant laboratory valuesErythrocytes
Hemoglobin
4.38 x 1012/L
142 g/L
4.02 x 1012/L
128 g/L
3.83 x 1012/L
109 g/L
Leukocytes4.2 x 109/L6.1 x 109/L7.6 x 109/L
Platelets170 x 109/L196 x 109/L129 x 109/L
Total bilirubin
PV-INR
AST
ALT
GGT
ALP
27 µmol/L
1.55
43 U/L
18 U/L
97 U/L
148 U/L
15 µmol/L
1.06
46 U/L
93 U/L
33 U/L
73 U/L
28 µmol/L
1.04
68 U/L
21 U/L
14 U/L
48 U/L
BUN
Creatinine
eGFR
10.5 mmol/L
114 µmol/L
66 mL/min/1,73 m2
8.5 mmol/L
113 µmol/L
64 mL/min/1,73 m2
16.9 mmol/L
243 µmol/L
25 mL/min/1,73 m2
NT-proBNP
Troponin I
6759 ng/L
172.7 ng/L
5407 ng/L
105.5 ng/L
4101 ng/L
37.0 ng/L
Posttransplant eventsSurgicalPericardial effusionPericardial effusionProlonged peritoneal drainage
Pericardial effusion
InfectiveNoneNoneNone
NeoplasticNoneNoneNone
Organ rejectionEarly cellular liver graft rejectionNoneNone
Graft organ functionBoth preservedBoth preservedBoth preserved
Donor-specific antibodiesTransient low intensityNoneNone

Conclusion: Dual organ transplantation is a viable option in selected patients with favorable outcomes when managed appropriately. This case series from the UHC Zagreb highlights the importance of individualized care and follow-up to optimize survival and graft function. Further studies are needed to standardize protocols for these complex procedures.

LITERATURE

1 

Itagaki S, Toyoda N, Moss N, Mancini D, Egorova N, Mikami T, et al. Outcomes of Simultaneous Heart and Kidney Transplantation. J Am Coll Cardiol. 2023 February 28;81(8):729–40. https://doi.org/10.1016/j.jacc.2022.11.053 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/36813371

2 

Guendouz S, Grimbert P, Radu C, Cherqui D, Salloum C, Mongardon N, et al. Heart Transplantation, Either Alone or Combined With Liver and Kidney, a Viable Treatment Option for Selected Patients With Severe Cardiac Amyloidosis. Transplant Direct. 2022 June 17;8(7):e1323. https://doi.org/10.1097/TXD.0000000000001323 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/35747521

3 

Huang X, Salerno D, Kovac D, Scheffert J, Hedvat J, Carver B, et al. Contemporary Immunosuppression Management and 1-Year Outcomes in Dual Organ Heart Transplantation. Clin Transplant. 2024 August;38(8):e15420. https://doi.org/10.1111/ctr.15420 PubMed: http://www.ncbi.nlm.nih.gov/pubmed/39113661


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