Kidney Transplantation From Deceased Donors With Bloodstream Infection: A Multicenter Retrospective Study

Hyejin Mo; Juhan Lee; Jae Berm Park; Sun Cheol Park; Young Hoon Kim; Ahram Han; In Mok Jung; Jongwon Ha; Nam-Joong Kim; Sangil Min

doi:10.3346/jkms.2022.37.e4

Journal List > J Korean Med Sci > v.37(1) > 1148799

Go to TopGo to Top Go to BottomGo to Bottom

TOOLS

Mo, Lee, Park, Park, Kim, Han, Jung, Ha, Kim, and Min: Kidney Transplantation From Deceased Donors With Bloodstream Infection: A Multicenter Retrospective Study

Original Article

Infectious Diseases, Microbiology & Parasitology

Journal of Korean Medical Science 2021; 37(1): e4.

Published online: 29 November 2021

DOI: https://doi.org/10.3346/jkms.2022.37.e4

Kidney Transplantation From Deceased Donors With Bloodstream Infection: A Multicenter Retrospective Study

Hyejin Mo¹

, Juhan Lee²

, Jae Berm Park³

, Sun Cheol Park⁴

, Young Hoon Kim⁵

, Ahram Han⁶

, In Mok Jung¹

, Jongwon Ha^6,⁷

, Nam-Joong Kim⁸

, Sangil Min⁶

¹Department of Surgery, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Korea.

²Department of Surgery, Yonsei University College of Medicine, Seoul, Korea.

³Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

⁴Department of Surgery, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.

⁵Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

⁶Department of Surgery, Seoul National University College of Medicine, Seoul, Korea.

⁷Transplantation Research Institute, Seoul National University College of Medicine, Seoul, Korea.

⁸Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.

Address for Correspondence: Sangil Min, MD, PhD. Department of Surgery, Seoul National University College of Medicine, 101 Daehak-ro, Jongno-gu, Seoul 03080, Korea. surgeonmsi@gmail.com

Received 23 July 2021 Accepted 11 November 2021

The Korean Academy of Medical Sciences

https://creativecommons.org/licenses/by-nc/4.0/

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

The use of organs from donors with infection is limited because of the possibility of transmission. We aimed to investigate the transmission after deceased donor transplantation with bloodstream infection (BSI).

Methods

A retrospective study of patients undergoing kidney or pancreas transplantation at five tertiary centers in Korea from January 2009 and November 2019 was performed. We analyzed the outcomes after transplantation from deceased donors with BSI.

Results

Eighty-six recipients received transplantation from 69 donors with BSI. The most common isolated pathogens from donors were Gram-positive bacteria (72.0%), followed by Gram-negative bacteria (22.7%), and fungi (5.3%). Appropriate antimicrobial agents were used in 47.8% of donors before transplantation. Transmission occurred only in 1 of 83 recipients (1.2%) from bacteremic donors and 1 of 6 recipients (16.7%) from fungemic donors. One-year patient and graft survival was 97.5%and 96.3%, respectively. There was no significant difference in graft and patient survival between patients who received organs from infected donors and noninfected donors.

Conclusion

Using organs from donors with bacteremia seems to be a safe option with low transmission risk. The overall prognosis of using organs from donors with BSI is favorable.

Graphical Abstract

Keywords: Retrospective Studies, Bacteremia, Fungi, Kidney Transplantation

INTRODUCTION

Transplantation using organs from donors with bloodstream infection poses a risk of transmission. It has been shown that there is no need to turn down the kidneys from donors labeled increased risk for disease transmission; however, it is still cautious about using allografts from donors who have already been confirmed to be infected.1 Generally, the transmission is reported in less than 1% of deceased donor donations.2 Besides, several successful transplant cases have been reported from the donors even with virulent pathogens or severe infection.3 4 5 6

Nevertheless, the fact that donor-derived infections are still associated with high morbidity and mortality makes decision-making difficult.7 8 9 And in the RESITRA study, which prospectively searched for bacterial infections, the transmission rate is relatively higher than that of other studies.9 This means that the transmission is affected by reporting; in other words, it may have been underrated.

There is a major limitation in studying transmission as a single-center study. Because donors with bloodstream infections account for only 5% of all donors and a center usually does not receive both organs, it is difficult to know the exact transmission rate.10 Therefore, we aimed to evaluate the transmission rate and transplant outcomes by conducting a multicenter retrospective study from 5 tertiary medical centers, which perform approximately 30% of deceased donor transplant in Korea.

METHODS

Study population

The Korean Network for Organ Sharing (KONOS) is a government-affiliated organization that handles deceased donor organ transplantation data in South Korea. Data were extracted from the database of Tissue and Blood Management Department under KONOS. This database was used to identify recipients who received transplants from donors with abnormal blood culture tests from January 2009 to November 2019. Based on their age, sex, transplant date, and aortic cross-clamp time, patients who underwent kidney and simultaneous pancreas-kidney transplant at Seoul National University Hospital, Severance Hospital, Samsung Medical Center, Seoul St. Mary’s Hospital, and Asan Medical Center were identified. In addition, patients who were not listed in the KONOS database and received transplants from infected donors at these 5 tertiary medical centers were identified additionally. Among them, patients with available microbiology reports were included in the analysis.

Data collection and definition

KONOS data was used only for the identification of the study population and for information about the use of antibiotics in donors. All other data were obtained from the medical record of each hospital.

We collected data, including donors’ age, sex, cause for death, length of intensive care unit stay, recipients’ age, sex, original disease, human leukocyte antigen (HLA) mismatch number, and cold ischemic time. Data on pathogens isolated in donor blood culture, the number of cultures, and susceptibility test results were collected.

After transplantation, the following outcomes were reviewed. Within one year after transplant, all infectious complications and associated pathogens and clinical course of infectious complications were recorded. During the same period, the occurrence of acute rejection and related anti-rejection treatment were reviewed. Graft function at one year, graft, and patient survival were collected.

If the criteria for proven or probable transmission were satisfied, it was confirmed as a transmission event. Proven transmission was defined when there was clear evidence of the same infection disease in the donor and at least one of the recipients. Probable transmission was defined when there was strong evidence suggesting but not proving a disease transmission.11 Further details can be found in the published paper.8 Before transplant, appropriate antimicrobial therapy was defined as when antimicrobial agents susceptible to bacteria or fungi growing in donor blood were used at least 24 hours before organ retrieval. After transplant, appropriate antimicrobial therapy was defined as when used at least 48 hours in recipients. Delayed graft function (DGF) is defined as the need for renal replacement therapy within the first week after transplantation.12

Statistical analysis

Normally distributed continuous variables were expressed as mean ± SD, and non-normally distributed ones were expressed as median and range. Logistic regression modeling was used to explore the factors affecting infectious complications. To compare graft and patient survival between the infected donor group and the non-infected donor group, we matched these two in a 1:3 fashion using the propensity score. Propensity scores were calculated using donor age, sex, recipient age, sex, HLA mismatch, presence of donor-specific antibody, and transplant type. Statistical analyses were performed using SPSS (version 23.0; SPPS Inc., Chicago, IL, USA). A value of P < 0.05 was considered statistically significant.

Ethics statement

This study was conducted in accordance with the Declaration of Helsinki and was approved by the Seoul National University Hospital, Severance Hospital, Samsung Medical Center, Seoul St. Mary’s Hospital, and Asan Medical Center Institutional Review Board (2002-173-1107). Informed consent was waived for this study by these IRBs.

RESULTS

Patients

During the assessed period, a total of 277 deceased donors with abnormal blood culture tests were identified in the KONOS database. Kidney and pancreas allografts from these donors were transplanted in 577 recipients. A total of 179 recipients were confirmed to receive transplants at 5 tertiary centers. Excluding patients with inadequate microbiologic results, 86 recipients who received transplants from 69 donors with positive microbiology results were included in the analysis.

Patient demographics are shown in Table 1. The mean ages of the donors were 43.1 ± 16.4 years, with 63.8% male. The mean length of intensive care unit stay of 69 donors was 12.0 ± 12.6 days, and 47.8% of donors received appropriate antimicrobial agents before retrieval operation. The mean duration of cold ischemia was 245.6 ± 99.9 minutes. 34.9% of recipients received induction therapy with thymoglobulin.

Table 1

Donor, recipient and transplant characteristics

Variables			Values
Donor (n = 69)
	Age, yr		43.1 ± 16.4
	Male		44 (63.8)
	Cause of death
		Cerebrovascular diseases	30 (43.5)
		Anoxia	23 (33.3)
		Brain trauma	16 (23.2)
	ICU stay, day		12.0 ± 12.6
	Use of appropriate antimicrobial therapy before retrieval operation		33 (47.8)
Recipient (n = 86)
	Age, yr		46.9 ± 15.1
	Male		53 (61.6)
	Cause of chronic kidney disease
		Unknown	21 (24.4)
		Diabetic nephropathy	19 (22.1)
		IgA nephropathy	11 (12.8)
		Hypertensive nephropathy	9 (10.5)
		Glomerulonephritis	9 (10.5)
		FSGS	4 (4.7)
		Polycystic kidney disease	5 (5.8)
		Other	8 (9.3)
Organ transplanted
	Kidney		83 (96.5)
	Simultaneous pancreas–kidney		3 (3.5)
Transplantation
	Cold ischemia time, min		245.6 ± 99.9
	HLA mismatch		2.8 ± 1.8
	Induction
		Basiliximab	56 (64.0)
		Thymoglobulin	31 (34.9)

Data are shown as mean ± SD or number (%).

ICU = intensive care unit, IgA = immunoglobulin A, FSGS = focal segmental glomerulosclerosis, HLA = human leukocyte antigen.

Microbiology

The microbiologic results are summarized in Table 2. All microorganisms were isolated from donors’ blood. Gram-positive bacteria and gram-negative bacteria accounted for 72.0% and 22.7%, respectively. Fungemia was confirmed in 4 donors. Six patients had polymicrobial infections (Candida parapsilosis and Staphylococcus epidermidis; Staphylococcus haemolyticus and Staphylococcus capitis; Enterococcus avium and Candida tropicalis; Enterococcus faecium and Klebsiella pneumoniae; Enterococcus faecium and Staphylococcus aureus; Staphylococcus haemolyticus and Staphylococcus cohnii). Coagulase-negative Staphylococcus was the most common organism isolated in donors’ blood. In 25 donors, two or more cultures were positive; in 25 donors, only one of the multiple blood culture results was positive, and information on the number of cultures was not available in the rest.

Table 2

List of organisms isolated from donors’ blood

Organisms			No. of patients (%)
Gram positive
	Streptococcus viridans		4 (5.3)
	Staphylococcus aureus		6 (8.0)
	Enterococcus species		7 (9.3)
	Coagulase-negative Staphylococcus
		Staphylococcus epidermidis	9 (12.0)
		Staphylococcus hemolyticus	7 (9.3)
		Staphylococcus capitis	5 (6.7)
		Staphylococcus cohnii	3 (4.0)
		Staphylococcus hominis	1 (1.3)
		Unspecified	3 (4.0)
	Others		9 (12.0)
Gram negative
	Klebsiella pneumoniae		5 (6.7)
	Escherichia coli		4 (5.3)
	Acinetobacter baumannii		3 (4.0)
	Pseudomonas aeruginosa		3 (4.0)
	Stenotrophomonas maltophilia		1 (1.3)
	Others		1 (1.3)
Fungi
	Candida		4 (5.3)

Outcomes

The organisms identified in the recipient within 1 year after transplant are summarized in Table 3. The most common infection site was the urinary tract, and the most frequently identified pathogen was Escherichia coli. The next most frequent site of infection was the abdominal cavity, followed by the pulmonary and bloodstream. Most infectious events occurred early after transplantation (Fig. 1).

Table 3

Pathogens associated with infectious complications in recipients within 1 year after transplant

Organisms	Bloodstream	Urinary	Abdominal	Pulmonary	Other
Escherichia coli	2	8	1	1	1
Klebsiella pneumoniae	2	3	1	3	0
Pseudomonas aeruginosa	0	2	0	1	0
Enterobacter cloacae	0	2	0	0	0
Enterococcus species	1	4	3	0	1
Staphylococcus aureus	0	1	1	0	1
Coagulase negative Staphylococci	0	0	1	0	0
Streptococcus viridans	1	0	1	0	0
Candida species	1	1	1	1	0
Others	0	4	2	2	0
Total	7	25	11	8	3
Time of infection onset, days after transplantation	47.0 (12.0–89.0)	45.0 (12.0–78.0)	25.0 (16.0–43.0)	19.5 (8.5–40.8)	76.0 (31–227)

Values are presented as median (interquartile range).

Fig. 1

Kaplan-Meier cumulative probability curve showing the incidence of infectious complications after transplantation.

One (1.2%) of the 83 recipients was suspected of bacterial transmission and the fungal transmission was confirmed in 1 (16.7%) of 6 recipients (Table 4). A 58-year-old male (recipient 1) received a kidney from the donor with carbapenem-resistant Acinetobacter baumannii bacteremia and subsequently developed urinary tract infection with the same organism early after transplantation. After 7 days of targeted antibiotic therapy, the infection resolved without clinical sequelae. A 60-year-old male (recipient 2) had received adequate antifungal therapy for seven days due to the candidemia of the donor. However, a month after transplant, persistent candidemia and infected endocarditis developed and required surgical treatment. The patient was followed up for 21 months, the renal function was stable (the last creatinine level was 1.54 mg/dL), and there were no additional infection episodes.

Table 4

Clinical course of the recipients with transmission events

Donor	Pathogen from donor’s blood	Antibiotics therapy before organ retrieval (preoperative days)	Organ transplanted	Recipient	Antibiotics after transplant (postoperative days)	Transmission	Clinical course	Serum creatinine (mg/dL) at 1 year	Patient survival at 1 year
Donor 1 (M/33)	Carbapenem-resistant Acinetobacter baumannii	Ceftriaxone (18–12) Piperacillin/tazobactam (12) Vancomycin (5) Tigecycline (< 1) Colistin (< 1)	Kidney	Recipient1 M/58	Colistin (7)	Urinary tract infection at POD 12	Improved after antibiotics therapy without sequelae	1.51	Alive
Donor 2 (M/62)	Candida tropicalis	Piperacillin/tazobactam (10–2) Meropenem (2) Linezolid (< 1)	Kidney	Recipient2 M/60	Linezolid (6) Fluconazole (7)	Candidemia developed POD 47	Persistent candidemia and infected endocarditis revolved after antifungal treatment and mitral valve debridement and irrigation	1.66	Alive

Specific antibiotics according to the susceptibility profiles are shown in bold.

After propensity matching, the baseline characteristic between the infected donor group and the noninfected donor group is shown in Table 5. One-year outcomes are summarized in Table 6.

Table 5

Demographic, clinical and immunological data of the studied population

Variables			After propensity score matching		P value
Transplant year 2009–2014			Infected donor (n = 38)	Noninfected donor (n = 114)
	Donor
		Male	20 (52.6)	68 (59.6)	0.448
		Age, yr	41.5 ± 16.5	42.2 ± 16.5	0.812
	Recipient
		Male	20 (52.6)	59 (51.8)	0.925
		Age, yr	46.4 ± 14.3	46.6 ± 17.0	0.922
		HLA mismatch	3.0 ± 1.6	3.2 ± 1.6	0.537
		Positive donor-specific antibody	2 (5.3)	8 (7.0)	1.000
		Kidney transplant	37 (97.4)	112 (98.2)	1.000
Transplant year 2015–2019			Infected donor (n = 48)	Noninfected donor (n = 144)
	Donor
		Male	36 (75.0)	101 (70.1)	0.519
		Age, yr	43.3 ± 18.0	44.2 ± 18.1	0.768
	Recipient
		Male	33 (68.8)	100 (69.4)	0.928
		Age, yr	47.7 ± 15.7	48.0 ± 17.8	0.931
		HLA mismatch	2.6 ± 1.9	2.6 ± 2.0	0.768
		Positive donor-specific antibody	2 (4.2)	4 (2.8)	0.641
		Kidney transplant	46 (95.8)	142 (98.6)	0.261

Data are shown as mean ± SD or number (%).

HLA = human leukocyte antigen.

Table 6

One-year outcomes of recipients from infected donors and non-infected donors

Variables		Infected donor (n = 86)	Noninfected donor (n = 258)	P value
Delayed graft function		19 (22.1)	34 (13.2)	0.047
Acute rejection		17 (19.8)	49 (19.0)	0.886
Graft function
	Creatinine, mg/dL	1.4 ± 0.6	1.3 ± 0.5	0.166
	eGFR, mL/min/1.73 m²	58.8 ± 29.2	61.3 ± 20.1	0.400
Allograft survival, %		96.3	96.8	0.541
Patient survival, %		97.5	98.4	0.465

Values are presented as number (%).

eGFR = estimated glomerular filtration rate.

In recipients of organs from infected donors, 22.1% of patients developed DGF after transplant. The mean serum creatinine and evaluated glomerular filtration rate at one year were 1.4 ± 0.9 mg/dL and 58.1 ± 29.6 mL/min/1.73 m², respectively. Except for the rates of DGF, there were no significant differences in outcomes, including graft survival and patient survival (Fig. 2), between recipients from infected and noninfected donors.

Fig. 2

Patient survival (A) and graft survival (B) by donor infection.

DISCUSSION

The shortage of organs is a constant problem in transplantation, and there have been various efforts to increase the donor pool. Infection in donors is not a rare condition, and it is found in about 20% of donors.13 It was found that bacteremia was detected in about 5% of deceased donors,10 and Candida species were detected in preservation fluid in about 0.1% of cases.14 Even if there is an active or suspected infection in the donor, it is recommended to consider the use of allograft based upon the urgency of transplantation for the recipient, the availability of alternative organs, and recipient informed consent.15 However, transmission is still a concern because it is known that transmission is associated with a poor prognosis.7 8 The biggest obstacle to knowing the exact rate of transmission is that there are many cases where the donor and recipient are in different organizations, and communication between them is limited and not prompt.8 Thus, there may be cases where it is not clear whether it is a transmission or de novo infection.

Although some cases of bacterial transmission are reported, the outcomes of using donors with bacterial infection are mostly favorable. In a study using the United Network for Organ Sharing (UNOS) database, there was no difference in graft survival and patient survival except the occurrence of DGF between recipients who received kidney transplants from blood culture positive donors (n = 3,646) and propensity score-matched recipients from non-blood culture-positive donors.16 In addition, several single-center studies have demonstrated that bacterial transmission is infrequent.17 18 19 Similar to previous studies using the UNOS database, some studies have shown that infectious complications, graft, and patients survival are not significantly different between infected and non-infected donors.17 20 The transmission was mostly reported in case reports. Most of them were related to multidrug-resistant pathogens or were not receiving appropriate antimicrobial agents due to unexpected infection.21 22 23 24 However, even in the case of multidrug-resistant bacteria, it was emphasized that transmission did not occur if antimicrobial agents were properly used for seven days after the recognition of the donor infection.25 Our study showed the same results. If donors have bloodstream bacterial infection, our study showed that the transmission rate is very rare. Although the use of appropriate antimicrobial agents was in less than half (47.8% before transplant and 39.5% after transplant), no bacterial transmission was reported.

For fungal infections, there is a more lack of data. Although fungal transmission was quite rare, it seemed to be associated with worse results than bacterial transmission.26 In a multicenter study conducted in France, Candida species were detected at the kidney graft site in 0.1% of cases, and 75% of recipients were infected Candida species.14 Most of the recipients with transmitted infections had serious complications such as aneurysms or graft loss. For fungal infections other than Candida species, the incidence is not well known. Most infections are not detected in routine screening; therefore, there have been some cases with serious consequences due to insufficient treatment.24 27 28 If multiple infections occur in recipients received from common donors, it is recommended to share this information immediately, treat patients appropriately, and observe them for an extended period of time. In our study, Candida species was confirmed in the donor's blood, not the graft site, and transmission occurred in 1 (16.7%) of the 6 cases. The recipient received proper antifungal treatment for seven days after transplant; however, the infection was not controlled even with an empirical antifungal agent. Therefore, the patient received surgical treatment due to infected endocarditis.

Our study has some limitations. The first limitation of this study is its retrospective design. The second is the small number of patients, which shows the limitation of the KONOS database. Currently, KONOS database only collects infection data up to the time of transplantation, so patients with confirmed infections after transplantation may have been excluded. Especially for fungal infections, it was difficult to draw definite conclusions because the number of patients was small. Third, there were some cases where central nervous system only grew in one of several donor blood cultures. Although it was not definite whether it was a true pathogen or not, it was considered true pathogens because it was accompanied by fever, and there was no other infection site. Another limitation is that the data on the culture of preservation fluid is not routinely collected in Korea. Previous studies showed that positive preservation fluid culture was associated with an increased risk of transmission.14 29 In Korea since the cold ischemic time is short in most cases, it is thought that graft-site infection incidence may be slightly lower, but it has not been accurately evaluated.

In conclusion, using organs from donors with bacteremia seems to be a safe option with a low risk of transmission. However, whether to use organs from donors with fungemia should be cautiously determined.

Notes

Disclosure: The authors have no potential conflicts of interest to disclose.

Author Contributions:

Conceptualization: Mo H, Min S.
Data curation: Mo H, Lee J, Park J, Park S, Kim Y, Han A, Jung I, Ha J, Min S.
Formal analysis: Mo H, Lee J, Park J, Park S, Kim Y.
Supervision: Min S.
Writing - original draft: Mo H.
Writing - review & editing: Mo H, Kim N, Min S.

References

1. Bowring MG, Holscher CM, Zhou S, Massie AB, Garonzik-Wang J, Kucirka LM, et al. Turn down for what? Patient outcomes associated with declining increased infectious risk kidneys. Am J Transplant. 2018; 18(3):617–624. PMID: 29116674.

2. Ison MG, Hager J, Blumberg E, Burdick J, Carney K, Cutler J, et al. Donor-derived disease transmission events in the United States: data reviewed by the OPTN/UNOS Disease Transmission Advisory Committee. Am J Transplant. 2009; 9(8):1929–1935. PMID: 19538493.

3. Caballero F, Lopez-Navidad A, Perea M, Cabrer C, Guirado L, Solà R. Successful liver and kidney transplantation from cadaveric donors with left-sided bacterial endocarditis. Am J Transplant. 2005; 5(4 Pt 1):781–787. PMID: 15760402.

4. Cohen J, Michowiz R, Ashkenazi T, Pitlik S, Singer P. Successful organ transplantation from donors with Acinetobacter baumannii septic shock. Transplantation. 2006; 81(6):853–855. PMID: 16570007.

5. Goldberg E, Bishara J, Lev S, Singer P, Cohen J. Organ transplantation from a donor colonized with a multidrug-resistant organism: a case report. Transpl Infect Dis. 2012; 14(3):296–299. PMID: 22176504.

6. Ariza-Heredia EJ, Patel R, Blumberg EA, Walker RC, Lewis R, Evans J, et al. Outcomes of transplantation using organs from a donor infected with Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae . Transpl Infect Dis. 2012; 14(3):229–236. PMID: 22624726.

7. Wan Q, Liu H, Ye S, Ye Q. Confirmed transmission of bacterial or fungal infection to kidney transplant recipients from donated after cardiac death (DCD) donors in China: a single-center analysis. Med Sci Monit. 2017; 23:3770–3779. PMID: 28771455.

8. Ison MG, Nalesnik MA. An update on donor-derived disease transmission in organ transplantation. Am J Transplant. 2011; 11(6):1123–1130. PMID: 21443676.

9. Len O, Gavaldà J, Blanes M, Montejo M, San Juan R, Moreno A, et al. Donor infection and transmission to the recipient of a solid allograft. Am J Transplant. 2008; 8(11):2420–2425. PMID: 18925908.

10. Lumbreras C, Sanz F, González A, Pérez G, Ramos MJ, Aguado JM, et al. Clinical significance of donor-unrecognized bacteremia in the outcome of solid-organ transplant recipients. Clin Infect Dis. 2001; 33(5):722–726. PMID: 11477528.

11. Garzoni C, Ison MG. Uniform definitions for donor-derived infectious disease transmissions in solid organ transplantation. Transplantation. 2011; 92(12):1297–1300. PMID: 21996654.

12. Mallon DH, Summers DM, Bradley JA, Pettigrew GJ. Defining delayed graft function after renal transplantation: simplest is best. Transplantation. 2013; 96(10):885–889. PMID: 24056620.

13. Corman Dincer P, Tore Altun G, Birtan D, Arslantas R, Sarici Mert N, Özdemir I, et al. Incidence and risk factors for systemic infection in deceased donors. Transplant Proc. 2019; 51(7):2195–2197. PMID: 31378467.

14. Albano L, Bretagne S, Mamzer-Bruneel MF, Kacso I, Desnos-Ollivier M, Guerrini P, et al. Evidence that graft-site candidiasis after kidney transplantation is acquired during organ recovery: a multicenter study in France. Clin Infect Dis. 2009; 48(2):194–202. PMID: 19090753.

15. Wolfe CR, Ison MG. AST Infectious Diseases Community of Practice. Donor-derived infections: guidelines from the American Society of Transplantation Infectious Diseases Community of Practice. Clin Transplant. 2019; 33(9):e13547. PMID: 30903670.

16. Huaman MA, Vilchez V, Mei X, Davenport D, Gedaly R. Donor positive blood culture is associated with delayed graft function in kidney transplant recipients: a propensity score analysis of the UNOS database. Clin Transplant. 2016; 30(4):415–420. PMID: 26840885.

17. Freeman RB, Giatras I, Falagas ME, Supran S, O'Connor K, Bradley J, et al. Outcome of transplantation of organs procured from bacteremic donors. Transplantation. 1999; 68(8):1107–1111. PMID: 10551637.

18. González-Segura C, Pascual M, García Huete L, Cañizares R, Torras J, Corral L, et al. Donors with positive blood culture: could they transmit infections to the recipients? Transplant Proc. 2005; 37(9):3664–3666. PMID: 16386498.

19. Yuan X, Chen C, Zhou J, Han M, Wang X, Wang C, et al. Organ donation and transplantation from donors with systemic infection: a single-center experience. Transplant Proc. 2016; 48(7):2454–2457. PMID: 27742320.

20. Outerelo C, Gouveia R, Mateus A, Cruz P, Oliveira C, Ramos A. Infected donors in renal transplantation: expanding the donor pool. Transplant Proc. 2013; 45(3):1054–1056. PMID: 23622623.

21. Wendt JM, Kaul D, Limbago BM, Ramesh M, Cohle S, Denison AM, et al. Transmission of methicillin-resistant Staphylococcus aureus infection through solid organ transplantation: confirmation via whole genome sequencing. Am J Transplant. 2014; 14(11):2633–2639. PMID: 25250717.

22. Kieslichova E, Protus M, Nemcova D, Uchytilova E. Single mutidrug resistant enterobacteriacae donor-derived infection in four solid organ transplant recipients: a case report. BMC Surg. 2019; 19(1):111. PMID: 31412850.

23. Kumar D, Cattral MS, Robicsek A, Gaudreau C, Humar A. Outbreak of pseudomonas aeruginosa by multiple organ transplantation from a common donor. Transplantation. 2003; 75(7):1053–1055. PMID: 12698099.

24. Kim SH, Ha YE, Youn JC, Park JS, Sung H, Kim MN, et al. Fatal scedosporiosis in multiple solid organ allografts transmitted from a nearly-drowned donor. Am J Transplant. 2015; 15(3):833–840. PMID: 25639881.

25. Mularoni A, Bertani A, Vizzini G, Gona F, Campanella M, Spada M, et al. Outcome of transplantation using organs from donors infected or colonized with carbapenem-resistant gram-negative bacteria. Am J Transplant. 2015; 15(10):2674–2682. PMID: 25981339.

26. Singh N, Huprikar S, Burdette SD, Morris MI, Blair JE, Wheat LJ, et al. Donor-derived fungal infections in organ transplant recipients: guidelines of the American Society of Transplantation, Infectious Diseases Community of Practice. Am J Transplant. 2012; 12(9):2414–2428. PMID: 22694672.

27. Farnon EC, Kokko KE, Budge PJ, Mbaeyi C, Lutterloh EC, Qvarnstrom Y, et al. Transmission of Balamuthia mandrillaris by organ transplantation. Clin Infect Dis. 2016; 63(7):878–888. PMID: 27358357.

28. Baddley JW, Schain DC, Gupte AA, Lodhi SA, Kayler LK, Frade JP, et al. Transmission of cryptococcus neoformans by organ transplantation. Clin Infect Dis. 2011; 52(4):e94–e98. PMID: 21220771.

29. Yansouni CP, Dendukuri N, Liu G, Fernandez M, Frenette C, Paraskevas S, et al. Positive cultures of organ preservation fluid predict postoperative infections in solid organ transplantation recipients. Infect Control Hosp Epidemiol. 2012; 33(7):672–680. PMID: 22669228.

TOOLS

Similar articles