Skip to main content

Transplantation during the COVID-19 pandemic: nothing noble is accomplished without danger

Abstract

The global health crisis due to the fast spread of coronavirus disease (COVID-19) has caused major disruption in all aspects of healthcare. Transplantation is one of the most affected sectors, as it relies on a variety of services that have been drastically occupied to treat patients affected by COVID-19. With this report from two transplant centers in Italy, we aim to reflect on resource organization, organ allocation, virus testing and transplant service provision during the course of the pandemic and to provide actionable information highlighting advantages and drawbacks.

To what extent can we preserve the noble purpose of transplantation in times of increased danger? Strategies to minimize risk exposure to the transplant population and health- workers include systematic virus screening, protection devices, social distancing and reduction of patients visits to the transplant center. While resources for the transplant activity are inevitably reduced, new dilemmas arise to the transplant community: further optimization of time constraints during organ retrievals and implantation, less organs and blood products donated, limited space in the intensive care unit and the duty to maintain safety and outcomes.

Peer Review reports

Background

Since December 2019, the fast spread of the novel Severe Acute Respiratory Syndrome CoronaVirus-2 (SARS-CoV-2) causing a severe acute respiratory disease (COVID-19), has determined a healthcare crisis in a growing number of countries. To date, USA, Spain and Italy have reported the highest number of patients affected, and COVID-19 has been categorized as a global pandemic [1]. Disruptions in almost all aspects of health care provision have been observed, and health systems are trying to continue offering essential services while suspending those that can be postponed.

Transplant services can be categorized depending on their lifesaving nature. Heart, lung and liver transplants are urgent lifesaving operations in a proportion of wait-listed patients. In particular, those with chronic end-stage organ disease who develop deterioration of their baseline condition, and those who suffer from sudden end-stage failure of a given organ.

While it seems obvious that lifesaving transplant activity should not be stopped, it is not clear whether non-lifesaving transplants should be delayed past the most critical phase of the emergency. In fact, prolonging the time spent on the waiting list can translate into waiting list drop-out due to disease progression or overcoming contra-indications.

On May 3, 2020, Italy is the third most affected country worldwide and has registered the second highest number of COVID-19-related deaths so far. The Italian National Authority for Transplantation released guidance on donor and recipient testing for SARS-CoV-2 [2, 3]. Testing via naso-pharyngeal swab (NPS) or bronchoalveolar lavage and, if positive, measurement of viral load on blood sample are recommended in all donors from high incidence regions. SARS-CoV-2 positive potential deceased donors are to be discarded and living donors postponed. NPS is compulsory before transplantation for all potential recipients who are symptomatic or with a history of contact with a COVID-19 positive patient, and discretional for asymptomatic recipients in whom history of contact with COVID-19 positive patient can be reasonably ruled out.

Implications of the spread of COVID-19 for the transplant community are innumerable, and the unprecedented nature of the pandemic has left physicians without guidance in many of their management choices. Balancing resource constraints, patient safety and life-saving organs demand is difficult during COVID-19 pandemic. With the present report we aim to reflect on the open challenges for the transplant community. A summary of actions to be undertaken is summarized, reflecting on advantages and dangers related to each (Table 1).

Table 1 Summary of issues and actions to be undertaken to mitigate the risks for the transplant population and staff related to COVID-19

Screening and risk exposure for transplant staff

Since the beginning of the pandemic, health-workers screening has been advocated as an essential tool for: 1) protecting patients from staff-mediated transmission and 2) protecting health-workers allowing prompt treatment. In the setting of transplantation, the first is of paramount importance, being the immunosuppressed population more vulnerable to infections. As of February 11, 2020, out of 44,672 confirmed COVID-19 cases in Mainland China, 1716 (3.8%) cases were health-workers [4]. To date, 21,338 health-workers have tested positive for SARS-CoV-2 in Italy and 154 doctors (including retired ones) and 40 nurses lost their lives after being infected [5]. Shortage of personal protection devices and work overload have contributed to increase the rate of contagion within health-workers. Hosts of SARS-CoV-2 may transmit the virus while they are asymptomatic or during the incubation period, a mechanism that creates a vicious circle of in-hospital disease spread to patients and staff. Testing all the transplant staff (or, at least, those who come into contact with transplanted patients) could mitigate the risk of in-hospital transmission at the price of increased costs and workload for already under-pressure health systems. In Italy, during the fast-growing spread of COVID-19 in March, the lack of tests did not allow to adopt such an extensive screening policy.

In addition, transplant teams are at higher risk of contagion as they might travel to high incidence areas when retrieving organs for transplantation. Some countries do not have a centralized organ retrieval system and transplant teams travel outside their regions to procure organs they will implant. A “travelling organs” policy such as in the National Organ Retrieval System in the United Kingdom or Eurotransplant in central Europe help avoid transplant teams travelling from low to high incidence regions and contain the spread within medical staff. In our region, liver transplant centers based in Rome share an organ procurement scheme to retrieve and ship organs to other centers in Italy. Most regions in Italy have implemented a regional organ sharing system which, during the COVID-19 pandemic, has been increasingly utilized.

Timing and logistics of transplantation

Due to the relevant number of false negative viral tests, there is a consistent risk of transplanting recipients who are either asymptomatic or in the incubation phase. This mandates caution and candidates for transplantation are delayed if their condition allows to. However, countries where social distancing measures have been in place for as long as the median virus incubation time, have the opportunity to rule out possible false negative tests from recipients who have complied with the social restriction policy [6, 7].

Success of transplantation relies on optimization of time constraints. The additional time required for COVID-19 testing of donors and recipients may delay organ procurement and lower the utilization rate especially of hemodynamically unstable donors that normally require fast-track management to minimize organs damage. Machine perfusion for organ preservation is expanding in almost all solid organs transplantation, allowing extend preservation time in liver, kidney, lung and heart transplantation [8, 9]. Machine perfusion could come into help when organs need to be retrieved quickly and preserved while virus tests are processed, in particular in unstable donors with low-risk history for COVID-19.

In an effort to minimize the possibility of delays which cause prolongation of cold ischemia time, back-up transplant candidates have been called in as a routine policy by several transplant centers when issues with the first-choice candidate are anticipated. Implementing such policy during the COVID-19 outbreak could offer the possibility to quickly replace the first candidate if they turn out to be SARS-CoV-2 positive.

Remote outpatient clinics via telephone or video calls (tele-clinics) are increasingly utilized to reduce hospital congestion and seminal experiences in kidney transplantation have registered even higher attendance rates than conventional clinics in selected patients [10]. Converting a proportion of outpatient clinics appointments to tele-clinics may reduce transplant population exposure to the virus. Numbers of visits (even tele-visits) can be reduced selecting only those patients with new symptoms or active issues, delaying well-being ones. A policy of remote management of immunosuppression by testing immunosuppressant level in local laboratories (then transmitted electronically) can be encouraged, thus relieving the workload on transplant centers.

Virus tests and transplantation

In transplant services, a delay or failure to diagnose SARS-CoV-2 infection in a donor may potentially produce disastrous consequences for the recipient and also increase the risk for health-workers [11]. In this context, the role of in vitro diagnostics is crucial to screen donors and recipients. An appropriate diagnostic strategy for the detection of virus infection involves collecting the correct specimen from the patient at the right time and performing an accurate and rapid laboratory test (Table 2).

Table 2 Diagnostic tests available in Italy to detect SARS-CoV-2 infection

Reverse transcription-polymerase chain reaction

The gold standard technique for detecting the SARS-CoV-2 infection is the real-time polymerase chain reaction (RT-PCR). This test has the advantage that the primers required can be produced as soon as the viral sequence is known. RT-PCR provides high levels of diagnostic sensitivity and specificity but the test protocol of nucleic acid amplification is complex and requires specialized instruments and technicians [12]. Although SARS-COV-2 RNA has been detected from a variety of respiratory sources, US Centers for Disease Control and Prevention recommends collecting only the upper respiratory NPS [13]. This indication is in accordance with Wang et al., that reported good detection rates of SARS-CoV-2 RNA in NPS (63% of the examined samples) [14]. SARS-CoV-2 RNA has been also detected from feces and blood specimens, although less reliably than from respiratory specimens. Higher viral loads have been detected soon after symptoms onset; thus, respiratory specimens should be collected within the first 7 days. Missing the time-window of viral replication can cause false negative results [15, 16]. Several RT-PCR protocols for the detection of SARS-CoV-2 RNA have been released by the World Health Organization and nowadays are widely standardized. However, work overload and logistic difficulties to ship samples to the few specialized centers, lead to significant delays in response time (up to 4–5 days in remote hospitals) [17]. This has caused issues in transplant services where rapid tests are needed to accelerate clinical decision-making. Several new generation real-time RT-PCR protocols for the detection of SARS-COV-2 RNA have been recently developed. These assays are suitable for decentralized point-of-care use and allow obtaining reliable results within 1 h (actual state-of-the-art detection methods). One of these, Simplexa™ COVID-19 Direct (DiaSorin Molecular LLC, CA) received the FDA’s emergency use authorization and it is nowadays available in Italy. Simplexa™ incorporate nucleic acid extraction, amplification and detection together into an integrated system ensuring a simple, safe and highly qualitative test [18,19,20].

Serology

A recent study reported acute antibody responses to SARS-CoV-2 in 285 patients and clarified that antibodies produced during the course of infection by symptomatic and asymptomatic patients can aid to the diagnosis of COVID-19 [21]. Immunoassays for detection of SARS-COV-2 immunoglobulin (Ig) M and IgG antibodies have proven to be highly specific and sensitive providing diagnostic evidence of infection in a few minutes. Moreover, the use of serology rapid tests could facilitate the diagnosis of SARS-CoV-2 infections when the molecular assays were performed unsatisfactorily [22, 23]. Several companies, driven by the growing demand of healthcare systems started to produce rapid immunoassays for SARSCoV-2. The majority of these are solid phase immunochromatographic assays for the qualitative and differential detection in human whole blood, serum or plasma of IgG and IgM antibodies to SARS-CoV-2. Although the manufacturers guarantee an accuracy close to 100%, doubts exist in the scientific community about the time kinetics of humoral response and for the potential cross reactivity with other coronaviruses [24]. In our opinion, active surveillance with rapid serological tests may prove a good option for the screening of asymptomatic donors and recipients.

Transplant benefit during the pandemic

Limited resources allocation is the mainstay of patient care during catastrophes. When multiple casualties present at the same time, patients are triaged and treatments offered based on the chance of success. With the growing COVID-19 pandemic, the capacity of many intensive care units (ICU) has been saturated, which forced physicians to adopt a strict selection of patients who can be treated. Transplantation has always faced the issue of limited resources due to the scarcity of donors and the growing demand of organs. In liver transplantation, the concept of transplant benefit has gained wide acceptance in the last decade, in an effort to guarantee equity during organs allocation, counterbalancing the principles of utility (recipients with the highest chances of a good outcome) and urgency (recipients with the biggest need of transplantation) [25, 26].

The widespread of COVID-19 has already caused a drastic reduction in organ donation and this is predicted to aggravate further in the next months. Times of further restraints stimulate reconsidering principles of allocation and adopt a pragmatic approach based on the available resources. A drop in the availability of blood products due to the reduction in blood donors has been registered too. Restricting transplants only to the sickest recipients (unbalancing towards the “urgency” principle) could address the need of patients at imminent risk of death from end-stage organ failure. However, it is not known how this will increase mortality rates on the waiting list for all other patients who are delayed (i.e., those at “the bottom of the list”). As an example, patients with model for end-stage liver disease (MELD) of 30 have a 62% mortality rate without liver transplantation at 3 months while the rate drops to 25% with a MELD of 20. On the contrary, privileging liver transplant candidates with higher chances of success and therefore shorter hospital stay and lower consumption of blood transfusion (unbalancing towards the “utility” principle) would reduce the workload on ICUs, at the price of excluding the sickest candidates. Liver transplant recipients with MELD ≥30 have been shown to require about double the amount of perioperative blood transfusion and days of ICU stay compared to patients with MELD < 30 [27]. As happened in the past, it should be noted that waitlisted patients might be reluctant to undergo a transplant during the course of epidemics, especially those whose disease is not as severe to threaten life in the short-term [28].

A “phased approach” to decreasing transplant activity has been proposed, with varying degrees of reduction depending on resource availability [29]. In addition, for the continuation of a transplant programme, a “clean path” within the ICU has to be maintained and not all hospitals might be in a condition to offer it.

During the SARS outbreak in 2003 some transplant centers closed their activity temporarily and donor assessment guidelines were developed to mitigate the risk related to donor selection [30]. During the Ebola epidemic in 2014, the specifics of travel history of potential donors were thoroughly assessed by the organ procurement organizations. At that time, the high lethality of Ebola kept the number of affected people relatively low and the impact on organ donation was contained. The lack of effective treatments for Ebola stimulated the ethical debate around the value of the informed consent to transplantation in times of epidemics: a recipient might be willing to accept the risk of infection to gain the benefit of a new organ, however this does not contemplate the risk of infection spread to health-workers [31].

In the United Kingdom, the national authority for transplantation has released clinical advice on donation acceptance criteria (deceased donors will be considered only if < 50 and < 60 years of age respectively for circulatory- and brain-dead donors). Most non-lifesaving transplant programmes such as pancreas and living-donor kidney have been put on hold [32]. In Switzerland, almost all non-lifesaving transplants have been suspended. Other countries have advised in favor of a case-by-case decision on both donation and transplantation, depending on local conditions.

So far, most countries have reported a heterogeneous distribution of COVID-19 across their regions, with foci of high incidence of contagion causing major disruption to social life and healthcare. In a recently published article, Michaels et al. suggested to redistribute patients on the waiting list in endemic regions to less affected areas [33]. Such approach offers the advantage of not penalizing patients on the waiting list only because of their geographical distribution, however, in a rapidly changing scenario, less affected areas may need to keep their resources available for possible sudden increases in hospital beds demand.

Conclusions

COVID-19 pandemic is an unprecedented life-changing crisis causing disruption in all the aspects of social life, especially for the wealthier economies of the world. As our health systems are built around patient-centered care, a cultural switch towards society over individual benefit seems mandatory in order not to run out of resources and guarantee the survival of our communities [34]. Stringent measures have been put in place to control the disease spread. Transplantation is one of the biggest advances in medical care and achievements in human history, a noble discipline that has crossed dangerous paths for the sake of its development. In this time of global crisis, the whole transplant community is called to join forces and develop strategies to mitigate risks and continue delivering the best possible results with the available resources to the multitude of patients awaiting organs from all over the world.

Availability of data and materials

The data used and analyzed during the current study are extrapolated and available from the cited articles as listed in the “Reference” section. If requested by the editors, we will provide the data and information on which the conclusions of this manuscript are based.

Abbreviations

COVID-19:

Coronavirus disease-19

ICU:

Intensive care unit

Ig:

Immunoglobulin

MELD:

Model for end-stage liver disease

MERS:

Middle East respiratory syndrome

NPS:

Naso-pharyngeal swab

RNA:

Ribonucleic acid

RT-PCR:

Reverse transcription-polymerase chain reaction

SARS-CoV2:

Severe acute respiratory syndrome Coronavirus 2

References

  1. Coronavirus disease 2019 (COVID-19) Situation Report – 104. https://www.who.int/docs/default-source/coronaviruse/situation-reports/20200503-covid-19-sitrep-104.pdf?sfvrsn=53328f46_2 Accessed 3 May 2020.

  2. C_17_cntAvvisi_229_0_file.pdf. http://www.trapianti.salute.gov.it/imgs/C_17_cntAvvisi_229_0_file.pdf. Accessed 4 Apr 2020.

  3. C_17_cntAvvisi_234_0_file.pdf. http://www.trapianti.salute.gov.it/imgs/C_17_cntAvvisi_234_0_file.pdf. Accessed 4 Apr 2020.

  4. Team TNCPERE. The epidemiological characteristics of an outbreak of 2019 novel coronavirus diseases (COVID-19) — China, 2020. China CDC Wkly. 2020;2(8):113–22.

    Google Scholar 

  5. EpiCentro. Coronavirus | Istituto Superiore di Sanità. https://www.epicentro.iss.it/coronavirus/. Accessed 3 May 2020.

  6. Polak WG, Fondevila C, Karam V, et al. Impact of COVID-19 on liver transplantation in Europe: alert from an early survey of European liver and intestine transplantation association (ELITA) and European liver transplant registry (ELTR). Transpl Int. 2020. doi:https://doi.org/10.1111/tri.13680. Published online July 1, 2020.

  7. Akdur A, Karakaya E, Ayvazoglu Soy EH, et al. Coronavirus disease (COVID-19) in kidney and liver transplant patients: a single-center experience. Exp Clin Transplant. 2020;18(3):270–4. https://doi.org/10.6002/ect.2020.0193.

    Article  PubMed  Google Scholar 

  8. Lai Q, Melandro F, Rossi M, Ruberto F, Pugliese F, Mennini G. Role of perfusion machines in the setting of clinical liver transplantation: a qualitative systematic review. Clin Transpl. 2018;32(8):e13310. https://doi.org/10.1111/ctr.13310.

    Article  Google Scholar 

  9. Yeung JC, Krueger T, Yasufuku K, et al. Outcomes after transplantation of lungs preserved for more than 12 h: a retrospective study. Lancet Respir Med. 2017;5(2):119–24. https://doi.org/10.1016/S2213-2600(16)30323-X.

    Article  PubMed  Google Scholar 

  10. Udayaraj UP, Watson O, Ben-Shlomo Y, et al. Establishing a tele-clinic service for kidney transplant recipients through a patient-codesigned quality improvement project. BMJ Open Qual. 2019;8(2). https://doi.org/10.1136/bmjoq-2018-000427.

  11. Lai Q, Spoletini G, Bianco G, et al. SARS-CoV2 and immunosuppression: A double-edged sword. Transpl Infect Dis. 2020:e13404. https://doi.org/10.1111/tid.13404 Published online July 8, 2020.

  12. Loeffelholz MJ, Tang Y-W. Laboratory diagnosis of emerging human coronavirus infections - the state of the art. Emerg Microbes Infect. 2020:1–26. https://doi.org/10.1080/22221751.2020.1745095 Published online March 20, 2020.

  13. CDC. Coronavirus Disease 2019 (COVID-19). Centers for Disease Control and Prevention. Published February 11, 2020. https://www.cdc.gov/coronavirus/2019-ncov/lab/guidelines-clinical-specimens.html Accessed 27 Mar 2020.

  14. Wang W, Xu Y, Gao R, et al. Detection of SARS-CoV-2 in different types of clinical specimens. JAMA 2020. doi:https://doi.org/10.1001/jama.2020.3786. Published online March 11, 2020.

  15. Zou L, Ruan F, Huang M, et al. SARS-CoV-2 viral load in upper respiratory specimens of infected patients. N Engl J Med. 2020;382(12):1177–9. https://doi.org/10.1056/NEJMc2001737.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Wu JT, Leung K, Bushman M, et al. Estimating clinical severity of COVID-19 from the transmission dynamics in Wuhan, China Nat Med 2020:1–5. doi:https://doi.org/10.1038/s41591-020-0822-7. Published online March 19, 2020.

  17. National laboratories. https://www.who.int/emergencies/diseases/novel-coronavirus-2019/technical-guidance/laboratory-guidance. Accessed March 27, 2020.

  18. Chan JF-W, Yip CC-Y, To KK-W, et al. Improved molecular diagnosis of COVID-19 by the novel, highly sensitive and specific COVID-19-RdRp/Hel real-time reverse transcription-polymerase chain reaction assay validated in vitro and with clinical specimens. J Clin Microbiol 2020. doi:https://doi.org/10.1128/JCM.00310-20. Published online March 4, 2020.

  19. Lieberman JA, Pepper G, Naccache SN, Huang M-L, Jerome KR, Greninger AL. Comparison of commercially available and laboratory developed assays for in vitro detection of SARS-CoV-2 in clinical laboratories. J Clin Microbiol. 2020. https://doi.org/10.1128/JCM.00821-20 Published online April 29, 2020.

  20. Rhoads DD, Cherian SS, Roman K, Stempak LM, Schmotzer CL, Sadri N. Comparison of Abbott ID now, Diasorin Simplexa, and CDC FDA EUA methods for the detection of SARS-CoV-2 from nasopharyngeal and nasal swabs from individuals diagnosed with COVID-19. J Clin Microbiol. 2020. doi:https://doi.org/10.1128/JCM.00760-20. Published online April 17, 2020.

  21. Long Q-X, Liu B-Z, Deng H-J, et al. Antibody responses to SARS-CoV-2 in patients with COVID-19. Nat Med 2020. doi:https://doi.org/10.1038/s41591-020-0897-1. Published online April 29, 2020.

  22. Guo L, Ren L, Yang S, et al. Profiling early Humoral response to diagnose novel coronavirus disease (COVID-19). Clin Infect Dis 2020. doi:https://doi.org/10.1093/cid/ciaa310. Published online March 21.

  23. Sheridan C. Fast, portable tests come online to curb coronavirus pandemic. Nat Biotechnol, 2020. doi:https://doi.org/10.1038/d41587-020-00010-2. Published online March 23, 2020.

  24. Zhang W, Du R-H, Li B, et al. Molecular and serological investigation of 2019-nCoV infected patients: implication of multiple shedding routes. Emerg Microbes Infect. 2020;9(1):386–9. https://doi.org/10.1080/22221751.2020.1729071.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Schaubel DE, Guidinger MK, Biggins SW, et al. Survival benefit-based deceased-donor liver allocation. Am J Transplant. 2009;9(4 Pt 2):970–81. https://doi.org/10.1111/j.1600-6143.2009.02571.x.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Vitale A, Volk ML, De Feo TM, et al. A method for establishing allocation equity among patients with and without hepatocellular carcinoma on a common liver transplant waiting list. J Hepatol. 2014;60(2):290–7. https://doi.org/10.1016/j.jhep.2013.10.010.

    Article  PubMed  Google Scholar 

  27. Schlegel A, Linecker M, Kron P, et al. Risk assessment in high- and low-MELD liver transplantation. Am J Transplant. 2017;17(4):1050–63. https://doi.org/10.1111/ajt.14065.

    Article  CAS  PubMed  Google Scholar 

  28. Chui AKK, Rao ARN, Chan HLY, Hui AY. Impact of severe acute respiratory syndrome on liver transplantation service. Transplant Proc. 2004;36(8):2302–3. https://doi.org/10.1016/j.transproceed.2004.08.018.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Kumar D, Manuel O, Natori Y, et al. COVID-19: a global transplant perspective on successfully navigating a pandemic. Am J Transplant. 2020. doi:https://doi.org/10.1111/ajt.15876. Published online March 23, 2020.

  30. Kumar D, Tellier R, Draker R, Levy G, Humar A. Severe Acute Respiratory Syndrome (SARS) in a liver transplant recipient and guidelines for donor SARS screening. Am J Transplant. 2003;3(8):977–81. https://doi.org/10.1034/j.1600-6143.2003.00197.x.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Kaul DR, Mehta AK, Wolfe CR, Blumberg E, Green M. Ebola virus disease: implications for solid organ transplantation. Am J Transplant. 2015;15(1):5–6. https://doi.org/10.1111/ajt.13093.

    Article  CAS  PubMed  Google Scholar 

  32. COVID-19: Advice for Clinicians - ODT Clinical - NHS Blood and Transplant. https://www.odt.nhs.uk/deceased-donation/covid-19-advice-for-clinicians/. Accessed 26 Mar 2020.

  33. Michaels MG, La Hoz RM, Danziger-Isakov L, et al. Coronavirus disease 2019: Implications of emerging infections for transplantation. Am J Transplant 2020. doi:https://doi.org/10.1111/ajt.15832. Published online February 24, 2020.

  34. Nacoti M, Ciocca A, Giupponi A, et al. At the Epicenter of the Covid-19 Pandemic and Humanitarian Crises in Italy: Changing Perspectives on Preparation and Mitigation. NEJM Catal. 1(2). https://doi.org/10.1056/CAT.20.0080.

Download references

Acknowledgements

None.

Funding

This study was not supported by any funding.

Author information

Authors and Affiliations

Authors

Contributions

GS, GB, DG and QL were responsible for the conception, design and analysis of the study; GS, GB and DG were involved with the writing of the manuscript, collection and interpretation of data; QL was involved in the writing, reviewing and editing of the manuscript. All authors have read and approved the manuscript.

Corresponding author

Correspondence to Gabriele Spoletini.

Ethics declarations

Ethics approval and consent to participate

The study is a narrative review and represents the Authors’ opinions on the subject. Direct patient data collection and participants consent were not necessary.

Consent for publication

The study is a narrative review and represents the Authors’ opinions on the subject. Direct patient data collection and consent to publish were not necessary.

Competing interests

GS and QL are members of the editorial board (Associate Editor) of BMC Gastroenterology. GB and DG have no conflicts of interest to declare about the present study.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Spoletini, G., Bianco, G., Graceffa, D. et al. Transplantation during the COVID-19 pandemic: nothing noble is accomplished without danger. BMC Gastroenterol 20, 259 (2020). https://doi.org/10.1186/s12876-020-01401-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12876-020-01401-0

Keywords