Medical Policy
Policy Num: 07.003.014
Policy Name: Kidney Transplant
Policy ID: [07.003.014] [Ac / B / M+ / P+] [7.03.01]
Last Review: September 12, 2024
Next Review: September 20, 2025
Related Policies:
07.003.005 - Allogeneic Pancreas Transplant
08.001.014 - Chelation Therapy for Off-Label Uses
05.001.008 - Immunoglobulin Therapy
Population Reference No. | Populations | Interventions | Comparators | Outcomes |
1 | Individuals:
| Interventions of interest are:
| Comparators of interest are:
| Relevant outcomes include:
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2 | Individuals:
| Interventions of interest are:
| Comparators of interest are:
| Relevant outcomes include:
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Kidney transplant, a treatment option for end-stage renal disease, involves the surgical removal of a kidney from a cadaver, living-related donor, or living-unrelated donor and transplantation into the recipient.
For individuals who have end-stage renal disease without contraindications to kidney transplant who receive a kidney transplant from a living donor or deceased (cadaveric) donor, the evidence includes registry data and case series. Relevant outcomes are overall survival, morbid events, and treatment-related mortality and morbidity. Data from large registries have demonstrated reasonably high survival rates after kidney transplant for appropriately selected patients and significantly higher survival rates for patients undergoing kidney transplant compared with those who remained on a waiting list. Kidney transplantation is contraindicated for patients in whom the procedure is expected to be futile due to comorbid disease or in whom posttransplantation care is expected to significantly worsen comorbid conditions. The evidence is sufficient to determine that the technology results in a meaningful improvement in the net health outcome.
For individuals who have a failed kidney transplant without contraindications to kidney transplant who receive a kidney retransplant from a living donor or deceased (cadaveric) donor, the evidence includes registry data and case series. Relevant outcomes are overall survival, morbid events, and treatment-related mortality and morbidity. Data have demonstrated reasonably high survival rates after kidney retransplant (eg, 5-year survival rates ranging from 87% to 96%) for appropriately selected patients. Kidney retransplantation is contraindicated for patients for whom the procedure is expected to be futile due to comorbid disease or for whom posttransplantation care is expected to significantly worsen comorbid conditions. The evidence is sufficient to determine that the technology results in a meaningful improvement in the net health outcome.
Not applicable.
The objective of this evidence review is to determine situations in which a kidney transplant or kidney retransplant is medically appropriate and improves net health outcomes.
Kidney transplants with either a living or cadaver donor may be considered medically necessary for carefully selected candidates with end-stage renal disease.
Kidney retransplant after a failed primary kidney transplant may be considered medically necessary in patients who meet criteria for kidney transplantation.
Kidney transplant is considered investigational in all other situations.
Potential contraindications to solid organ transplant (subject to the judgment of the transplant center):
Known current malignancy, including metastatic cancer
Recent malignancy with high risk of recurrence
History of cancer with a moderate risk of recurrence
Systemic disease that could be exacerbated by immunosuppression
Untreated systemic infection making immunosuppression unsafe, including chronic infection
Other irreversible end-stage diseases not attributed to kidney disease
Psychosocial conditions or chemical dependency affecting ability to adhere to therapy
Indications for renal transplant include a creatinine level of greater than 8 mg/dL, or greater than 6 mg/dL in symptomatic diabetic patients; however, consideration for listing for renal transplant may start well before the creatinine level reaches this point, based on the anticipated time that a patient may spend on the waiting list.
Please see the Codes table for details.
Transplants, such as a kidney transplant, should be considered for coverage under the transplant benefit and should be evaluated for a charge in accordance with traditional transplant benefits.
Which expenses are incurred during the evaluation and procurement of organs and tissues should be compared with the scope of human organ transplant benefits for coverage determination. Typically, the following are considered human organ transplant benefits:
hospitalization of the recipient and living donor for medically recognized transplants from a donor to a transplant recipient;
evaluation tests requiring hospitalization to determine the suitability of both potential and actual donors, when such tests cannot be safely and effectively performed on an outpatient basis;
hospital room, board, and general nursing in semi-private rooms;
special care units, such as coronary and intensive care;
hospital ancillary services;
physicians' services for surgery, technical assistance, administration of anesthetics, and medical care;
acquisition, preparation, transportation, and storage of organ;
diagnostic services;
drugs that require a prescription by federal law.
Other examples of benefits include specific charges for participation in registries for organ procurement, operating rooms, supplies, use of hospital equipment, and transportation of the tissue or organ to be evaluated.
Administration of products with a specific transplant benefit needs to be defined as to:
when the benefit begins (at the time of admission for the transplant or once the patient is determined eligible for a transplant, which may include tests or office visits prior to transplant);
when the benefit ends (at the time of discharge from the hospital or at the end of the required follow-up, including the immunosuppressive drugs administered on an outpatient basis).
Coverage usually is not provided for:
human organ transplant services for which the cost is covered or funded by governmental, foundational, or charitable grants;
organs sold rather than donated to the recipient;
an artificial organ.
Benefits are determined by the group contract, member benefit booklet, and/or individual subscriber certificate in effect at the time services were rendered. Benefit products or negotiated coverages may have all or some of the services discussed in this medical policy excluded from their coverage.
Solid organ transplantation offers a treatment option for patients with different types of end-stage organ failure that can be lifesaving or provide significant improvements to a patient’s quality of life.1, Many advances have been made in the last several decades to reduce perioperative complications. Available data supports improvement in long-term survival as well as improved quality of life particularly for liver, kidney, pancreas, heart, and lung transplants. Allograft rejection remains a key early and late complication risk for any organ transplantation. Transplant recipients require life-long immunosuppression to prevent rejection. Patients are prioritized for transplant by mortality risk and severity of illness criteria developed by Organ Procurement and Transplantation Network (OPTN) and United Network of Organ Sharing (UNOS).
In 2023, 46,623 transplants were performed in the United States procured from 39,670 deceased donors and 6,948 living donors.2, Kidney transplants were the most common procedure with 27,332 transplants performed from both deceased and living donors in 2023. Since 1988, the cumulative number of kidney transplants is 581,744.3, Of the cumulative total, approximately 67% of the kidneys came from deceased donors and 33% from living donors.
Kidney transplant, using kidneys from deceased or living donors, is an accepted treatment of end-stage renal disease (ESRD). ESRD refers to the inability of the kidneys to perform their functions (ie, filtering wastes and excess fluids from the blood). ESRD, which is life-threatening, is also known as chronic kidney disease stage 5 and is defined as a glomerular filtration rate (GFR) less than 15 mL/min/1.73 m2.4, Patients with advanced chronic kidney disease, mainly stage 4 (GFR 15 to 29 mL/min/1.73 m2) and stage 5 (GFR <15 mL/min/1.73 m2), should be evaluated for transplant.5, Being on dialysis is not a requirement to be considered for kidney transplant. Severe non-compliance and substance abuse serve as contraindications to kidney transplantation but even those could be overcome with clinician support and patient motivation. All kidney transplant candidates receive organ allocation points based on waiting time, age, donor-recipient immune system compatibility, prior living donor status, distance from donor hospital, and survival benefit.6,7,
Combined kidney and pancreas transplants and management of acute rejection of kidney transplant using either intravenous immunoglobulin or plasmapheresis are discussed in separate evidence reviews.
Solid organ transplants are a surgical procedure and, as such, are not subject to regulation by the U.S. Food and Drug Administration (FDA).
The FDA regulates human cells and tissues intended for implantation, transplantation, or infusion through the Center for Biologics Evaluation and Research, under Code of Federal Regulation Title 21, parts 1270 and 1271. Solid organs used for transplantation are subject to these regulations.
This evidence review was created in December 1995 and has been updated regularly with searches of the PubMed database. The most recent literature update was performed through June 14, 2024.
Evidence reviews assess the clinical evidence to determine whether the use of technology improves the net health outcome. Broadly defined, health outcomes are the length of life, quality of life, and ability to function including benefits and harms. Every clinical condition has specific outcomes that are important to patients and managing the course of that condition. Validated outcome measures are necessary to ascertain whether a condition improves or worsens; and whether the magnitude of that change is clinically significant. The net health outcome is a balance of benefits and harms.
To assess whether the evidence is sufficient to draw conclusions about the net health outcome of technology, 2 domains are examined: the relevance, and quality and credibility. To be relevant, studies must represent 1 or more intended clinical use of the technology in the intended population and compare an effective and appropriate alternative at a comparable intensity. For some conditions, the alternative will be supportive care or surveillance. The quality and credibility of the evidence depend on study design and conduct, minimizing bias and confounding that can generate incorrect findings. The randomized controlled trial (RCT) is preferred to assess efficacy; however, in some circumstances, nonrandomized studies may be adequate. Randomized controlled trials are rarely large enough or long enough to capture less common adverse events and long-term effects. Other types of studies can be used for these purposes and to assess generalizability to broader clinical populations and settings of clinical practice.
Promotion of greater diversity and inclusion in clinical research of historically marginalized groups (e.g., People of Color [African-American, Asian, Black, Latino and Native American]; LGBTQIA (Lesbian, Gay, Bisexual, Transgender, Queer, Intersex, Asexual); Women; and People with Disabilities [Physical and Invisible]) allows policy populations to be more reflective of and findings more applicable to our diverse members. While we also strive to use inclusive language related to these groups in our policies, use of gender-specific nouns (eg, women, men, sisters, etc.) will continue when reflective of language used in publications describing study populations.
The purpose of a kidney transplant in patients who have end-stage renal disease (ESRD) without contraindications to a kidney transplant is to provide a treatment option that is an alternative to or an improvement on existing therapies.
The following PICO was used to select literature to inform this review.
The therapy being considered is kidney transplant from a living or cadaveric donor.
The following therapies and practices are currently being used to make decisions about managing ESRD: medical management, including dialysis and medications to control symptoms. Dialysis is an artificial replacement for some kidney functions. Dialysis is used as a supportive measure in patients who do not want kidney transplants or who are not transplant candidates; it can also be used as a temporary measure in patients awaiting a kidney transplant.
The general outcomes of interest are overall survival (OS), elimination of the need for dialysis, and treatment-related adverse events (eg, immunosuppression, graft failure, surgical complications, infections),with follow-up ranging from 30 days posttransplantation up to 10 years or more. See the Potential Contraindications section for detailed discussion.
Chaudhry et al (2022) published a systematic review that compared survival for waitlisted patients with kidney failure who received a transplant compared to those who remained on the transplant waitlist.8, A total of 48 observational studies were included in the systematic review, of which 18 studies were suitable for meta-analysis. Results demonstrated a 55% reduction in the risk of mortality in patients who received a transplant compared to those who remained on dialysis (hazard ratio [HR], 0.45; 95% confidence interval [CI], 0.39 to 0.54; p<.001).
According to data analysis from the Organ Procurement and Transplantation Network (OPTN), between 2008 and 2015, the 1-year survival of patients undergoing an initial kidney transplant was 97.1% (95% CI, 96.9% to 97.2%).3, Five-year survival was 86.5% (95% CI, 86.2% to 86.8% ).
Krishnan et al (2015) published a study of 17,681 patients in a U.K. transplant database who received a kidney transplant or were on a list to receive a kidney transplant.9, Authors found significantly higher 1- and 5-year survival rates in patients who underwent a kidney transplant than in those who remained on dialysis (exact survival rates not reported).
The UNOS proposed an Expanded Criteria Donor (ECD) approach in 2002 to include brain-dead donors over 60 years or between 50 and 59 years old with 2 or more of the following criteria: serum creatinine level greater than 1.5 mg/dL, death caused by cerebrovascular accident, or history of high blood pressure.10,
Querard et al (2016) conducted a systematic review and meta-analysis of studies comparing survival outcomes with ECD versus Standard Criteria Donor (SCD) kidney transplant recipients.10, Reviewers identified 32 publications, 5 of which adjusted for potential confounding factors. A pooled analysis of 2 studies reporting higher rates of patient-graft failure for ECD kidney recipients found a significantly higher adjusted HR for patient-graft survival (HR, 1.68; 95% CI, 1.32 to 2.12). Meta-analyses were not conducted for patient survival outcomes; however, 1 study (N=189) found a higher but nonsignificant difference in patient survival with ECD than with SCD (HR, 1.97; 95% CI, 0.99 to 3.91) and another study (N=13833) found a significantly increased risk of death with ECD than with SCD (HR, 1.25; 95% CI, 1.12 to 1.40).
Pestana (2017) published a retrospective, single-center analysis of kidney transplants performed between 1998 and 2015 at a hospital in Brazil.11, Of the 11,436 transplants analyzed, 31% (n=3614) were performed under SCD, while 14% (n=1618) were performed under ECD. The number of ECD recipients increased over time, from 29 transplants in 1998 to 2000 to 450 transplants from 2013 to 2014. Patient survival with ECD increased from 1998 to 2002 to 2011 to 2014 (from 79.7% to 89.2%, p<.001); a similar increase was noted in patient survival with SCD over the same time periods (from 73.1% to 85.2%, p<.001). The study was limited by reliance on limited registry data.
Several studies have reported long-term outcomes in live kidney donors. The most appropriate control group to evaluate whether donors have increased risks of morbidity and mortality are individuals who meet the criteria for kidney donation but who did not undergo the procedure. These types of studies have provided mixed findings. For example, Segev et al (2010) found that donors had an increased mortality risk.12, The authors analyzed data from a national registry of 80,347 live donors in the U.S. who donated organs between April 1994 and March 2009 and compared their data with data from 9364 participants of the National Health and Nutrition Examination Survey (excluding those with contraindications to kidney donation). There were 25 deaths within 90 days of live kidney donation during the study period. Surgical mortality from live kidney donors was 3.1 per 10,000 donors (95% CI, 2.0 to 4.6) and did not change over time, despite differences in practice and selection. Long-term risk of death was no higher for live donors than for age- and comorbidity-matched National Health and Nutrition Examination Survey III participants for all patients and also stratified by age, sex, and race.
Patients infected with human immunodeficiency virus (HIV) may receive organs from HIV-positive donors under approved research protocols through the HIV Organ Policy Equity Act. As of November 2017, 6 hospitals performed 34 such transplants (23 kidney and 11 liver transplants), involving organs from 14 deceased donors. In a prospective, nonrandomized study, Muller et al (2015) noted that HIV-positive patients transplanted with kidneys from donors testing positive for HIV showed a 5-year survival rate of 74%.13, Researchers noted that the HIV infection remained well-controlled and the virus was undetectable in the blood after transplantation.
Locke et al (2015) examined outcomes in 499 HIV-positive kidney transplant recipients identified in the Scientific Registry of Transplant Recipients.14, Compared with early era transplants (2004-2007), patients transplanted more recently (2008-2011) had a significantly lower risk of death (HR, 0.59; 95% CI, 0.39 to 0.90). The 5-year patient survival rate was 78.2% for patients transplanted in the early era and 85.8% for more recent transplants. In another study, Locke et al (2015) compared outcomes in 467 adult kidney transplant recipients with 4670 HIV-negative controls, matched on demographic characteristics.15, Compared with HIV-negative controls, survival among HIV-positive transplant recipients was similar at 5 years posttransplant (83.5% vs. 86.2%, p=.06). At 10 years, HIV-positive transplant recipients had a significantly lower survival rate (51.6%) than HIV-negative patients (72.1%; p<.001). The lower 10-year survival rate was likely due to HIV and hepatitis C virus (HCV) coinfection; survival rates at 10 years in HIV-monoinfected patients and HIV-negative patients were similar (88.7% vs. 89.1%, p=.50). Locke et al (2017) found significantly lower 5-year mortality rates in HIV-infected patients with ESRD who had kidney transplants compared with continued dialysis (adjusted relative risk [RR], 0.21; 95% CI, 0.10 to 0.42; p<.001).16,
In addition, Sawinski et al (2015) analyzed survival outcomes in patients infected with HIV, HCV, or HIV plus HCV.17, The analysis included 492 HIV-infected patients, 5605 HCV-infected patients, 147 coinfected patients, and 117,791 noninfected patients. In a multivariate analysis, compared with noninfected patients, HIV-infected patients did not have an increased risk of death (HR, 0.90; 95% CI, 0.66 to 1.24). However, HCV infection (HR, 1.44; 95% CI, 1.33 to 1.56) and HIV and HCV coinfection (HR, 2.26; 95% CI, 1.45 to 3.52) were both significantly associated with an increased risk of death.
Zheng et al (2019) performed a meta-analysis of 27 cohort studies, accounting for 1670 cases, to analyze various outcomes among HIV-positive patients who underwent kidney transplantation.18, The results revealed 97% (95% CI, 95% to 98%) survival at 1 year and 94% (95% CI, 90% to 97%) survival at 3 years. Other outcomes comprised 91% (95% CI, 88% to 94%) graft survival at 1 year, 81% (95% CI, 74% to 87%) graft survival at 3 years, 33% (95% CI, 28% to 38%) with acute rejections at 1 year, and 41% (95% CI, 34% to 50%) with infectious complications at 1 year.
Current OPTN policy permits HIV-positive transplant candidates.7,
The British HIV Association and the British Transplantation Society (2017) updated their guidelines on kidney transplantation in patients with HIV disease.19, These criteria may be extrapolated to other organs:
Adherent with treatment, particularly antiretroviral therapy
Cluster of differentiation 4 count greater than 100 cells/mL (ideally >200 cells/mL) for at least 3 months
Undetectable HIV viremia (<50 HIV-1 RNA copies/mL) for at least 6 months
No opportunistic infections for at least 6 months
No history of progressive multifocal leukoencephalopathy, chronic intestinal cryptosporidiosis, or lymphoma.
A meta-analysis by Fabrizi et al (2014) identified 18 observational studies comparing kidney transplant outcomes in patients with and without hepatitis C virus (HCV) infection.20, The studies included 133,350 transplant recipients. In an adjusted analysis, the risk of all-cause mortality was significantly higher in HCV-positive versus HCV-negative patients (RR, 1.85; 95% CI, 1.49 to 2.31). Risks were elevated in various study subgroups examined by investigators. When the analysis was limited to the 4 studies from the U.S., the adjusted RR was 1.29 (95% CI, 1.15 to 1.44). In an analysis of 10 studies published since 2000, the RR was 1.84 (95% CI, 1.45 to 2.34). An analysis of disease-specific mortality suggested that at least part of the increased risk in mortality among HCV-positive individuals must have been due to chronic liver disease. In a meta-analysis of 9 studies, the risk of liver disease-related mortality was considerably elevated in patients infected with HCV than in those uninfected (odds ratio, 11.6; 95% CI, 5.54 to 24.4).
In the analysis by Sawinski et al (2015), described above, HCV infection was associated with an increased risk of mortality in kidney transplant patients compared with noninfected patients.17,
Several studies have found that obese kidney transplant patients have improved outcomes compared with patients on a waiting list matched by body mass index (BMI). Study results on whether morbid obesity is associated with an increased risk of adverse events after kidney transplant are conflicting.
In an analysis of kidney transplant data from the U.K., Krishnan et al (2015) reported on BMI data for 13,536 patients.9, They devised several BMI categories (ie, <18.5 kg/m2, 18.5 to <25 kg/m2, 25 to <30 kg/m2, 30 to <35 kg/m2, and 35 to <40 kg/m2). For each BMI category, patient survival was significantly higher in those who underwent kidney transplants compared with those who remained on a waiting list. In a similar analysis of U.S. data, Gil et al (2013) noted that the risk of mortality at 1 year was significantly lower in patients who underwent transplantation than in those who remained on the waiting list for all BMI categories.21, For example, the risk was lower for patients with a BMI of at least 40 kg/m2 who received organs from donors who met standard criteria (HR, 0.52; 95 CI, 0.37 to 0.72) and for patients with BMI 35 to 39 kg/m2 who received organs from SCD donors (HR, 0.34; 95% CI, 0.26 to 0.46).
Pieloch et al (2014) retrospectively reviewed data from the OPTN database.22, The sample included 6055 morbidly obese patients (ie, BMI, 35 to 40 kg/m2) and 24,077 normal-weight individuals who underwent kidney transplant between 2001 and 2006. After controlling for potentially confounding factors, the overall 3-year patient mortality did not differ significantly between obese and normal-weight patients (HR, 1.03; 95% CI, 0.96 to 1.12). Similar results were found for 3-year graft failure (HR, 1.04; 95% CI, 0.98 to 1.11). In subgroup analyses, obese patients who were non-dialysis-dependent, nondiabetic, younger, receiving living donor transplants, and needing no assistance with daily living activities had significantly lower 3-year mortality rates than normal-weight individuals. For example, the odds for mortality between nondiabetic obese and normal-weight patients was 0.53 (95% CI, 0.44 to 0.63).
A multivariate analysis of the effect of obesity on transplant outcomes by Kwan et al (2016) included 191,091 patients from the Scientific Registry of Transplant Recipients database.23, Covariates in the analysis included age, sex, graft type, ethnicity, diabetes, peripheral vascular disease, dialysis time, and time period of transplantation. Multivariate regression analysis indicated that obese patients had a significantly increased risk of adverse transplant outcomes including delayed graft function, urine protein, acute rejection, and graft failure (p<.001 for all outcomes). The risk of adverse outcomes of obesity increased with increasing BMI (eg, see Table 1), and was independent of the effect of diabetes.
Body Mass Index, kg/m2 | Hazard Ratio | 95% Confidence Interval | p |
25 to 29.9 | 1.015 | 0.983 to 1.047 | .416 |
30 to 34.9 | 1.104 | 1.065 to 1.145 | <.001 |
35 to 39.9 | 1.216 | 1.158 to 1.276 | <.001 |
40+ | 1.248 | 1.156 to 1.348 | <.001 |
Kervinen et al (2018) looked at the probability of receiving renal transplantation and survival after transplantation for patients with type 2 diabetes mellitus (T2DM).24, Using the Finnish Registry for Kidney Diseases, which included 5419 patients between the years 2000 and 2010, 1065 individuals with T2DM were identified, of which 105 received a kidney transplant during follow-up. The relative probability of renal transplantation was 0.25 (95% CI, 0.20 to 0.30; p<.001) for T2DM patients compared with non-diabetic patients. Survival probabilities at 5 years after transplantation were 88% for T2DM and 93% for non-diabetic patients (adjusted HR for death 1.39, 95% CI, 0.82 to 2.35; p=.227). The limitations of this study were the relatively small number of T2DM patients receiving kidney transplantation and almost all of these were from deceased donors. Also, the transplantation criteria for T2DM patients in Finland may give better survival rates in the study.
Lim et al (2017) evaluated all-cause mortality following kidney transplantation in patients with T2DM from the Australia and New Zealand Dialysis and Transplant Registry.25, Of 10,714 transplant recipients during the study period, 985 (9%) had T2DM. The 10-year unadjusted OS in patients with an intact graft was 53% for individuals who had diabetes compared with 83% for transplant recipients who did not. The adjusted HR for all-cause mortality in patients with diabetes was 1.60 (95% CI, 1.37 to 1.86; p<.001), with the excess risk of death attributable to both cardiovascular disease and infection. Graft survival rates at 1, 5, and 10 years were 94%, 85%, and 70% in patients with diabetes compared with 95%, 89%, and 78% in transplant recipients without diabetes (p<.001), respectively.
A large number of kidney transplants have been performed worldwide. Available data have demonstrated reasonably high survival rates after kidney transplant for appropriately selected patients and significantly higher survival rates for patients undergoing kidney transplant compared with those who remained on a waiting list. HIV infection has not been found to increase the risk of adverse events after kidney transplantation. Obesity and T2DM may increase the risk of adverse outcomes, and some data have suggested that kidney transplant recipients with HCV have worse outcomes than those without hepatitis C infection; however, data have not shown that patients with these conditions do not benefit from kidney transplants.
For individuals who have end-stage renal disease without contraindications to kidney transplant who receive a kidney transplant from a living donor or deceased (cadaveric) donor, the evidence includes registry data and case series. Relevant outcomes are overall survival (OS), morbid events, and treatment-related mortality and morbidity. Data from large registries have demonstrated reasonably high survival rates after kidney transplant for appropriately selected patients and significantly higher survival rates for patients undergoing kidney transplant compared with those who remained on a waiting list. Kidney transplantation is contraindicated for patients in whom the procedure is expected to be futile due to comorbid disease or in whom posttransplantation care is expected to significantly worsen comorbid conditions. The evidence is sufficient to determine that the technology results in an improvement in the net health outcome.
Population Reference No. 1 Policy Statement | [X] MedicallyNecessary | [ ] Investigational |
The purpose of kidney retransplants in patients who have a failed kidney transplant without contraindications to another kidney transplant is to provide a treatment option that is an alternative to or an improvement on existing therapies.
The following PICO was used to select literature to inform this review.
The relevant population of interest are individuals with a failed kidney transplant without contraindications to another kidney transplant.
The therapy being considered is kidney retransplant from a living or cadaveric donor.
The following therapies and practices are currently being used to make decisions about managing patients whose kidney transplant has failed: medical management including dialysis, self-care, and medications, including dietary supplements and diuretics.
The general outcomes of interest are OS, elimination of the need for dialysis, and treatment-related adverse events (eg, immunosuppression, graft failure, surgical complications, infections), with follow-up ranging from immediate postsurgery to 30 days posttransplantation and long-term follow-up out to 10 years or more. See the Potential Contraindications section for detailed discussion.
Methodologically credible studies were selected using the following principles:
To assess efficacy outcomes, comparative controlled prospective trials were sought, with a preference for RCTs;
In the absence of such trials, comparative observational studies were sought, with a preference for prospective studies;
To assess long-term outcomes and adverse events, single-arm studies that capture longer periods of follow-up and/or larger populations were sought;
Studies with duplicative or overlapping populations were excluded.
Barocci et al (2009) in Italy reported on long-term survival after kidney retransplantation.26, There were 100 (0.8%) second transplants of 1302 kidney transplants performed at a single-center between 1983 and 2007. Among the second kidney recipients, 1-, 5-, and 10-year patient survival rates were 100%, 96%, and 92%, respectively. Graft survival rates at 1, 5, and 10 years were 85%, 72%, and 53%, respectively.
Kainz et al (2022) investigated the association of time on waitlist with survival in patients who received a second transplant versus those who remained on the waitlist.27, A total of 2346 patients from the Austrian Dialysis and Transplant Registry and Eurotransplant were retrospectively analyzed. Results demonstrated that retransplantation improved survival at 10 years of follow-up compared with remaining on the waitlist (HR for mortality, 0.73; 95% CI, 0.53 to 0.95). For patients with a waitlist time for retransplantation of <1 and 8 years after first graft loss, the mean survival time differences at 10 years were 8.0 life months gained (95% CI, 1.9 to 14.0) and 0.1 life months gained (95% CI, -14.3 to 15.2), respectively.
According to data analysis from the OPTN between 2008 and 2015, the 1-year survival rate of patients undergoing a repeat kidney transplant was 97.2% (95% CI, 96.8% to 97.5%).3, The 5-year patient survival rate after a repeat kidney transplant was 88.2% (95% CI, 87.4% to 88.9% ).
Gupta et al (2015) retrospectively analyzed OPTN data, focusing on patients who had an initial kidney transplant as children.28 A total of 2281 patients were identified who had their first transplant when they were younger than 18 years and a second kidney transplant at any age. In multivariate analysis, the length of first graft survival and age at second graft were significantly associated with second graft survival. Specifically, the first graft survival time of more than 5 years was associated with better second graft survival. However, patients who were between 15 and 20 years old at second transplant were at increased risk of second kidney graft failure compared with patients in other age groups.
Shelton et al (2017) evaluated outcomes in HIV-infected patients undergoing kidney retransplantation.29, In adjusted survival analysis, HIV-infected retransplant patients had a significantly increased risk of death compared with HIV-negative patients (HR=3.11; 95% CI, 1.82 to 5.34). Other factors significantly associated with increased risk of death after kidney retransplantation included recipient infection with HCV (HR=1.77; 95% CI, 1.32 to 2.38) and grafts from older donors (HR=1.01; 95 CI, 1.00 to 1.02). The analysis included only 22 HIV-infected patients, which is too small to draw conclusions about the appropriateness of kidney retransplantation in HIV-infected individuals.
Other contraindications are discussed in the section on initial kidney transplants.
Data have demonstrated reasonably high survival rates after kidney retransplants for appropriately selected patients (eg, 5-year survival rates ranging from 87% to 96%).
For individuals who have a failed kidney transplant without contraindications to kidney transplant who receive a kidney retransplant from a living donor or deceased (cadaveric) donor, the evidence includes registry data and case series. Relevant outcomes are OS, morbid events, and treatment-related mortality and morbidity. Data have demonstrated reasonably high survival rates after kidney retransplant (eg, 5-year survival rates ranging from 87% to 96%) for appropriately selected patients. Kidney retransplantation is contraindicated for patients for whom the procedure is expected to be futile due to comorbid disease or for whom posttransplantation care is expected to significantly worsen comorbid conditions. The evidence is sufficient to determine that the technology results in an improvement in the net health outcome.
Population Reference No. 2 Policy Statement | [X] MedicallyNecessary | [ ] Investigational |
The purpose of the following information is to provide reference material. Inclusion does not imply endorsement or alignment with the evidence review conclusions.
Guidelines or position statements will be considered for inclusion in ‘Supplemental Information' if they were issued by, or jointly by, a US professional society, an international society with US representation, or National Institute for Health and Care Excellence (NICE). Priority will be given to guidelines that are informed by a systematic review, include strength of evidence ratings, and include a description of management of conflict of interest.
In 2011, the American Society of Transplant Surgeons, the American Society of Transplantation, the Association of Organ Procurement Organizations, and the UNOS issued a joint position statement recommending modifications to the National Organ Transplant Act of 1984 .30, . The joint recommendation stated that the potential pool of organs from HIV-infected donors should be explored. With modern antiretroviral therapy, the use of these previously banned organs would open an additional pool of donors to HIV-infected recipients. The increased pool of donors has the potential to shorten waiting times for organs and decrease the number of waiting list deaths. The organs from HIV-infected deceased donors would be used for transplant only with patients already infected with HIV. In 2013, the HIV Organ Policy Equity Act permitting the use of this group of organ donors.
Not applicable.
The Medicare Benefit Policy Manual includes a chapter on ESRD.31, A section on identifying candidates for transplantation (140.1) states:
"After a patient is diagnosed as having ESRD , the physician should determine if the patient is suitable for transplantation. If the patient is a suitable transplant candidate, a live donor transplant is considered first because of the high success rate in comparison to a cadaveric transplant. Whether one or multiple potential donors are available, the following sections provide a general description of the usual course of events in preparation for a live-donor transplant."
Some currently unpublished trials that might influence this review are listed in Table 2.
NCT No. | Trial Name | Planned Enrollment | Completion Date |
Ongoing | |||
NCT04182607 | Donor Outcomes Following Hand-Assisted And Robotic Living Donor Nephrectomy: A Retrospective Review | 240 | Nov 2022 |
Unpublished | |||
NCT03500315 | HOPE in Action Prospective Multicenter, Clinical Trial of Deceased HIVD+ Kidney Transplants for HIV+ Recipients | 209 | May 2024 |
Codes | Number | Description |
---|---|---|
CPT | 50300 | Donor nephrectomy (including cold preservation), from cadaver, unilateral or bilateral |
50320 | As above, but from living donor | |
50323 | Backbench standard preparation of cadaver donor renal allograft prior to transplantation, including dissection and removal of perinephric fat, diaphragmatic and retroperitoneal attachments, excision of adrenal gland, and preparation of ureter(s), renal vein(s), and renal artery(s), ligating branches as necessary | |
50325 | Backbench standard preparation of living donor renal allograft (open or laparoscopic) prior to transplantation, including dissection and removal of perinephric fat and preparation of ureter(s), renal vein(s), and renal artery(s), ligating branches as necessary | |
50327 | Backbench reconstruction of cadaver or living donor renal allograft prior to transplantation; venous anastomosis, each | |
50328 | arterial anastomosis, each | |
50329 | ureteral anastomosis, each | |
50340 | Recipient nephrectomy | |
50360 | Renal allotransplantation; implantation of graft without recipient nephrectomy | |
50365 | As above, but with recipient nephrectomy | |
50547 | Laparoscopy, surgical; donor nephrectomy (including cold preservation) from living donor | |
HCPCS | No Code | |
ICD-10-CM | N18.1-N18.9 | Chronic kidney disease (CKD) code range |
ICD-10-PCS | 0TT00ZZ | Surgical, resection of right kidney, open |
0TT04ZZ | Surgical, resection of right kidney, percutaneous endoscopic | |
0TT10ZZ | Surgical, resection of left kidney, open | |
0TT14ZZ | Surgical, resection of left kidney, percutaneous endoscopic | |
0TY00Z0 | Surgical, transplantation of right kidney, allogeneic, open approach | |
0TY10Z0 | Surgical, transplantation of left kidney, allogeneic, open approach | |
Type of service | Surgery | |
Place of service | Inpatient |
As per Correct Coding Guidelines
Date | Action | Description |
---|---|---|
9/12/2024 | Annual Review | Policy updated with literature review through June 14, 2024; no references added. Policy statements unchanged. |
9/07/2023 | Annual Review | Policy updated with literature review through June 14, 2023; no references added. Policy statements unchanged. Paragraph for promotion of greater diversity and inclusion in clinical research of historically marginalized groups was added to Rationale section. |
90/8/2022 | Annual Review | Policy updated with literature review through June 10, 2022; references added. Minor editorial refinements to policy statements; intent unchanged. |
9/16/2021 | Annual Review | Policy updated with literature review through July 1, 2021; no references added. Policy statements unchanged. |
9/11/2020 | Policy newly adopted by Triple S | Policy with literature reviewed through June 15, 2020; references added. Policy statements unchanged based on already existed BCBS policy. |