Coverage Policy Manual
Policy #: 1998102
Category: Surgery
Initiated: August 2017
Last Review: October 2024
  Transplant, Allogeneic Islet Cell or Pancreas for Diabetes Mellitus

Description:
Transplantation of a healthy pancreas is a treatment for patients with insulin-dependent diabetes. Pancreas transplantation can restore glucose control and prevent, halt, or reverse the secondary complications from diabetes.
 
The American Diabetes Association has developed guidelines for pancreas transplantation. This coverage policy for pancreas transplantation follows these guidelines.
 
Allogeneic islet cell transplantation with donislecel-jujn is being investigated as a treatment or cure for patients with type 1 diabetes.
 
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 (Black, 2018). 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 the Organ Procurement and Transplantation Network and United Network of Organ Sharing.
 
In 2023, 46,630 transplants were performed in the United States procured from more than 16,000 deceased donors and 6,900 living donors (UNOS, 2024). Pancreas-kidney transplants were the fifth most common procedure, with 812 transplants performed in 2023. Pancreas-alone transplants were the sixth most common procedure, with 102 transplants performed in 2023.
 
Pancreas transplantation occurs in several different scenarios such as (1) a diabetic patient with renal failure who may receive a simultaneous cadaveric pancreas plus kidney transplant; (2) a diabetic patient who may receive a cadaveric or living-related pancreas transplant after a kidney transplantation (pancreas after kidney); or (3) a nonuremic diabetic patient with specific severely disabling and potentially life-threatening diabetic problems who may receive a pancreas transplant alone.
 
Data from the United Network for Organ Sharing and the International Pancreas Transplant Registry indicate that the proportion of simultaneous pancreas plus kidney transplant recipients worldwide who have type 2 diabetes has increased over time, from 6% of transplants between 2005 and 2009 to 9% of transplants between 2010 and 2014 (Gruessner, 2016). Between 2010 and 2014, approximately 4% of pancreas after kidney transplants and 4% of pancreas alone transplants were performed in patients with type 2 diabetes. In 2022, patients with type 2 diabetes accounted for 22.4% of all pancreas transplants, according to data from the Organ Procurement and Transplantation Network and the Scientific Registry of Transplant Recipients (Kandaswamy, 2024).
 
Allogeneic islet transplantation potentially offers an alternative to whole-organ pancreas transplantation in patients with type 1 diabetes (Vantyghem, 2019). In the case of allogeneic islet cell transplantation, cells are harvested from a deceased donor's pancreas, processed, and injected into the recipient's portal vein. Islet transplantation has generally been reserved for patients with frequent and severe metabolic complications who have consistently failed to achieve control with insulin-based management. Allogeneic transplantation may be performed in the radiology department.
 
In 2000, a modified immunosuppression regimen increased the success of allogeneic islet transplantation. This regimen is known as the "Edmonton protocol."
 
Regulatory Status
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 U.S. Food and Drug Administration (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. Allogeneic islet cells and solid organs for transplantation are included in these regulations. Donislecel-jujn (Lantidra™), a first-in-class deceased donor-derived allogeneic pancreatic islet cellular therapy product, was approved by the FDA in June 2023 for the treatment of type 1 diabetes in adults who are unable to approach target hemoglobin A1c due to repeated episodes of severe hypoglycemia despite intensive diabetes management and education (U.S. FDA, 2023).
 
 
Reimbursement for solid organ transplant (that has been pre-authorized if that is required) is made as a global fee limited to the lesser of billed charges or the average allowable charge authorized by the Blue Quality Centers for Transplant in the geographic region where the transplant is performed. This global payment includes all related transplant services including institutional, professional, ancillary, and organ procurement. The global period begins one day prior to the date of the transplant and continues for 23 days (for pancreas only) or 32 days (for a combination pancreas/kidney transplant) after the transplant. This covers the inpatient/outpatient stay and provides a per diem outlier payment if necessary. This global fee also includes the cost of complications arising from the original procedure when services are rendered within the global postoperative period for the particular transplant.
 
Coding
See CPT/HCPCS Code section below.
 
Note: G0341, G0342, and G0343 are codes used to report Medicare services that are part of a clinical trial and are not covered.
 
Related Policies
Coverage Policy #2003014, Transplant, Autologous Islet Cell for Chronic Pancreatitis, provides additional information

Policy/
Coverage:
Effective November 2023
 
Meets Primary Coverage Criteria Or Is Covered For Contracts Without Primary Coverage Criteria
 
*Note: A positive Hepatitis C status of organs for transplant is NOT a contraindication for transplant.
 
Pancreas transplantation meets member benefit certificate primary coverage criteria that there be scientific evidence of effectiveness and is covered in insulin dependent diabetic patients with imminent or established end-stage renal disease who have had or plan to have a kidney transplant, because the successful addition of a pancreas does not jeopardize patient survival, may improve kidney survival, and will restore normal glycemia. Such patients also must meet the medical indications and criteria for kidney transplantation and not have excessive surgical risk for the dual transplant procedure. The pancreas transplant may be done simultaneous with, or subsequent to, a kidney transplant.
 
In the absence of indications for kidney transplantation, pancreas transplantation is only covered for patients who meet the following three criteria:
 
    • A history of frequent, acute, and severe metabolic complications (hypoglycemia, hyperglycemia, ketoacidosis) requiring medical attention and documented in medical records;
    • Clinical and emotional problems with exogenous insulin therapy that are so severe as to be incapacitating; and
    • Consistent failure of insulin-based management to prevent acute complications.  
 
Pancreas re-transplant following a failed primary transplant is covered one time only, as there is no information available that more than one transplant attempt following the primary transplant is successful.
  
Does Not Meet Primary Coverage Criteria Or Is Investigational For Contracts Without Primary Coverage Criteria
 
Pancreatic islet cell transplants when done as an allogeneic transplant for a patient with diabetes mellitus does not meet member benefit certificate primary coverage criteria that there be scientific evidence of effectiveness.
 
For members with contracts without primary coverage criteria, pancreatic islet cell transplants when done as an allogeneic transplant for a patient with diabetes mellitus is considered investigational. Investigational services are specific contract exclusions in most member benefit certificates of coverage.
 
Allogeneic islet cell transplantation does not meet member benefit certificate primary coverage criteria that there be scientific evidence of effectiveness, including allogeneic islet transplantation using an FDA-approved cellular therapy product (donislecel-jujn [ie, Lantidra]) for the treatment of type 1 diabetes.
 
For members with contracts without primary coverage criteria, allogeneic islet cell transplantation is considered investigational including allogeneic islet transplantation using an FDA-approved cellular therapy product (donislecel-jujn [ie, Lantidra]) for the treatment of type 1 diabetes. Investigational services are specific contract exclusions in most member benefit certificates of coverage.
 
Islet transplantation with donislecel-jujn does not meet member benefit certificate primary coverage criteria that there be scientific evidence of effectiveness for any indication not listed as covered in this or other policies.
 
For members with contracts without primary coverage criteria, islet transplantation with donislecel-jujn is considered investigational for any indication not listed as covered in this or other policies. Investigational services are specific contract exclusions in most member benefit certificates of coverage.
 
Note: G0341, G0342, and G0343 are codes used to report Medicare services that are part of a clinical trial and are not covered.
 
Effective May 2019 – October 2023
 
Meets Primary Coverage Criteria Or Is Covered For Contracts Without Primary Coverage Criteria
 
*Note: A positive Hepatitis C status of organs for transplant is NOT a contraindication for transplant.
 
Pancreas transplantation meets primary coverage criteria for effectiveness and is covered in insulin dependent diabetic patients with imminent or established end-stage renal disease who have had or plan to have a kidney transplant, because the successful addition of a pancreas does not jeopardize patient survival, may improve kidney survival, and will restore normal glycemia.  Such patients also must meet the medical indications and criteria for kidney transplantation and not have excessive surgical risk for the dual transplant procedure.  The pancreas transplant may be done simultaneous with, or subsequent to, a kidney transplant.
 
In the absence of indications for kidney transplantation, pancreas transplantation is only covered for patients who meet the following three criteria:
 
    • A history of frequent, acute, and severe metabolic complications (hypoglycemia, hyperglycemia, ketoacidosis) requiring medical attention and documented in medical records;
    • Clinical and emotional problems with exogenous insulin therapy that are so severe as to be incapacitating; and
    • Consistent failure of insulin-based management to prevent acute complications.  
 
Pancreas re-transplant following a failed primary transplant is covered one time only, as there is no information available that more than one transplant attempt following the primary transplant is successful.
  
Does Not Meet Primary Coverage Criteria Or Is Investigational For Contracts Without Primary Coverage Criteria
 
Pancreatic islet cell transplants when done as an allogeneic transplant for a patient with diabetes mellitus does not meet primary coverage criteria for effectiveness.
 
For members with contracts without primary coverage criteria, pancreatic islet cell transplants when done as an allogeneic transplant for a patient with diabetes mellitus is considered investigational. Investigational services are specific contract exclusions in most member benefit certificates of coverage.
 
HCPCS codes G0341 (Percutaneous islet cell transplant, includes portal vein catheterization and infusion), G0342 (Laparoscopy for islet cell transplant, includes portal vein catheterization and infusion), and G0343 (Laparotomy for islet cell transplant, includes portal vein catheterization and infusion) were added effective October 1, 2004.  These codes are used to report Medicare services that are part of a clinical trial.  
 
Allogeneic islet cell transplantation does not meet primary coverage criteria for effectiveness.
 
For members with contracts without primary coverage criteria, allogeneic islet cell transplantation is considered investigational.  Investigational services are specific contract exclusions in most member benefit certificates of coverage.
 
Effective Prior to May 2019
 
Pancreas transplantation meets primary coverage criteria for effectiveness and is covered in insulin dependent diabetic patients with imminent or established end-stage renal disease who have had or plan to have a kidney transplant, because the successful addition of a pancreas does not jeopardize patient survival, may improve kidney survival, and will restore normal glycemia.  Such patients also must meet the medical indications and criteria for kidney transplantation and not have excessive surgical risk for the dual transplant procedure.  The pancreas transplant may be done simultaneous with, or subsequent to, a kidney transplant.
 
In the absence of indications for kidney transplantation, pancreas transplantation is only covered for patients who meet the following three criteria:
    • A history of frequent, acute, and severe metabolic complications (hypoglycemia, hyperglycemia, ketoacidosis) requiring medical attention and documented in medical records;
    • Clinical and emotional problems with exogenous insulin therapy that are so severe as to be incapacitating; and
    • Consistent failure of insulin-based management to prevent acute complications.  
 
Pancreas retransplant following a failed primary transplant is covered one time only, as there is no information available that more than one transplant attempt following the primary transplant is successful.
 
Pancreatic islet cell transplants are considered investigational when done as an allogeneic transplant for a patient with diabetes mellitus.  Investigational services are an exclusion in the member certificate of coverage.
 
HCPCS codes G0341 (Percutaneous islet cell transplant, includes portal vein catheterization and infusion), G0342 (Laparoscopy for islet cell transplant, includes portal vein catheterization and infusion), and G0343 (Laparotomy for islet cell transplant, includes portal vein catheterization and infusion) were added effective October 1, 2004.  These codes are used to report Medicare services that are part of a clinical trial.  
 
CPT category III codes 0141T, 0142T, and 0143T became active CPT codes on 1/1/06.
 
Allogeneic islet cell transplantation is not covered based on benefit certificate primary coverage criteria that there be scientific evidence of effectiveness.
 
For contracts without primary coverage criteria, allogeneic islet cell transplantation is considered investigational.  Investigational services are an exclusion in the member benefit contract.

Rationale:
Pancreas After Kidney (PAK) Transplant
Based on current pancreas transplant registry data, at nearly 3 years, 64% of transplant recipients have a functioning pancreas compared to 77% among recipients of simultaneous pancreas and kidney transplants. PAK transplantation allows the uremic patient the benefits of a living-related kidney graft, if available, and the benefits of a subsequent pancreas transplant that is likely to result in improved quality of life compared to a kidney transplant alone. Uremic patients for whom a cadaveric kidney graft is available but a pancreas graft is not simultaneously available benefit similarly from a later pancreas transplant.
 
Pancreas Transplant Alone (PTA)
PTA graft survival has improved in recent years; available data suggest that 60% of grafts are functioning at 2 years, with potential insulin independence. In carefully selected IDDM patients with severely disabling and potentially life-threatening complications due to hypoglycemia unawareness and labile diabetes that persists despite optimal medical management, the benefits of PTA were judged to outweigh the risk of performing pancreas transplantation with subsequent immunosuppression. The majority of patients undergoing PTA are those with either hypoglycemic unawareness or labile diabetes. However, other exceptional circumstances may exist where nonuremic IDDM patients have significant morbidity risks due to secondary complications of diabetes (i.e., peripheral neuropathy) that exceed those of the transplant surgery and subsequent chronic immunosuppression. Because there is virtually no published evidence regarding outcomes of medical management in this very small group of exceptional diabetic patients, it is not possible to generalize about which circumstances represent appropriate indications for pancreas transplantation alone. Case-by-case consideration of each patient’s clinical situation may be the best option for determining the balance of risks and benefits.
 
Pancreas Retransplantation
For all three types of pancreas transplant (i.e., pancreas transplant alone, simultaneous pancreas kidney transplant, and pancreas after kidney transplant), the survival of a second pancreas transplant was lower than for the primary transplant of the same type. However, patients receiving second pancreas transplants have a good chance of remaining insulin-independent for 3 years or more.  There are inadequate data to permit scientific conclusion regarding the health outcomes associated with third or subsequent pancreas transplants.
 
Islet Cell Transplantation
Allogeneic islet cell transplantation to treat type 1 diabetes has been investigated for over 20 years.  Allograft survival had been universally poor until A.M.J. Shapiro at the University of Alberta in Edmonton, Canada, developed what is now called the “Edmonton Protocol”.  An international multi-center trial using that protocol in 36 patients (out of 2000 screened for eligibility) reported that 1) 44% of patients attained the stringent primary end point of insulin independence (defined as a glycated hemoglobin value of less than 6.5%, a glucose level after an overnight fast not exceeding 140 mg/dL more than 3 times per week, and a 2-hour postprandial glucose level not exceeding 180 mg/dL more than 4 times a week); 2) 28% of patients had partial graft function; 3) and 28% had complete graft loss.  Unfortunately, 76% became insulin dependent again by 2 years after transplantation.
 
Only 10% of another 65 patients transplanted by the Edmonton group with the same protocol have maintained insulin independence after 5 years.
 
The American Diabetes Association has provided the following recommendation regarding islet cell transplants: "Pancreatic islet transplants hold significant potential advantages over whole-gland transplants.  Recent strides have been made in improving the suces rates of this procedure.  However, at this time, islet trnasplantation is a rapidly evolving technology that also requires systemic immunosuppression and should be performed only within the setting of controlled research studies."  Clinical trials on the effectiveness of allogeneic islet cell transplants are ongoing.
 
2011 Update
A search of the MEDLINE database was conducted through January 2011.  A summary of the updated literature is provided.
 
Changes to the pancreas and kidney allocation system in 2010 may positively affect the availability of both organs for simultaneous kidney/pancreas transplant and therefore reduce the need for pancreas after kidney transplant considerations in diabetic uremic patients. The inferior graft survival rate in PAK, however, may be improved with current immunosuppressive regimens. In 2009, Fridell and colleagues reported a retrospective review (n=203) of a single center’s experience with PAK and SPK since 2003, when current induction/tacrolimus immunosuppressive strategies became standard (Fridell, 2009). Of the cases studied, 61 (30%) were PAK and 142 (70%) were SPK. One-year patient survival rates were 98% and 95% (PAK and SPK, respectively; p=0.44). Pancreas graft survival rates at one year were observed to be 95% and 90%, respectively (p=0.28). The authors conclude that in the modern immunosuppressive era, PAK should be considered as an acceptable alternative to SPK in candidates with an available living kidney donor.
 
Data that suggest that SPK transplants have a higher overall graft survival rate than PAK, including kidney graft survival, has led to the question of whether kidney transplant alone (KTA) is superior to PAK. In 2009, Kleinclauss and colleagues retrospectively examined data from diabetic kidney transplant recipients (n=307) from a single center and compared renal graft survival rates in those who subsequently received a pancreatic transplant to those who did not (Kleinclauss, 2009). The comparative group was analyzed separately depending on whether they were medically eligible (KTA-E) for pancreas transplant, but chose not to proceed for financial or personal reasons, or were ineligible (KTA-I) for medical reasons. The KTA-I (n=57) group differed significantly at baseline from both the PAK group (n=175) and the KTA-E group (n=75) with respect to age, type of diabetes and dialysis experience; kidney graft survival rates were lower than either of the other groups, with one, five and 10-years rates of 75%, 54% and 22%, respectively (p<0.0001). The PAK and KTA-E groups were similar in age, race, type of diabetes, and dialysis experience. The authors compared one-, five- and ten-year kidney graft survival rates in PAK patients with those in the KTA-E group: 98%, 82% and 67% versus 100%, 84% and 62%, respectively, and concluded that the subsequent transplant of a pancreas after a living donor kidney transplant does not adversely affect patient or kidney graft survival rates.
 
The Pancreas Allotransplantation for Diabetic Nephropathy and Mild Chronic REnal fAilure Stage (PANCREAS) Study (NCT01067950) is currently recruiting participants at Nantes University in France. The stated objective of the study is to assess the superiority of isolated pancreas transplant to intensive insulin therapy in Type 1 diabetes patients with overt proteinuric nephropathy and mildly reduced renal function. This is to be an open-label, randomized trial. The primary combined endpoint is to be patient mortality and renal function impairment at five years. Secondary endpoints measuring safety and extrarenal diabetic complications are planned. If completed, this would represent the first RCT comparing pancreas transplant to insulin therapy.
 
In 2010, Mora and colleagues described the long-term outcome of 12 patients 15 years following simultaneous pancreas/kidney transplant (Mora, 2010). Metabolic measures of glucose control were measured at one, five, ten and 15 years following the procedure. Of this subset of patients, six (50%) had non-diabetic glucose challenge tests. Basal serum insulin levels declined over this period as well, from 24 mU/L to 16 mU/L at one and 15 years, respectively. The authors conclude that in a select group of patients whose pancreatic graft continued to function after 15 years, some glycemic control continued, albeit in a diminished fashion. It should be noted that this represents a small fraction of the 367 patients receiving the simultaneous pancreas/kidney transplant at this single center (12 of 367 SPK; 3.3%). The number of allograft survivals at five or more, and 10 or more years in this study was 43 (11.7%) and 28 (7.6%), respectively.
 
In 2009, Isla Pera and colleagues described the results of an observational quality of life (QoL) study in Spanish patients following SPK transplant (Isla Pera, 2009). Data on quality of life is particularly important in this patient population, due to the fact that alternatives to transplant exist, and quality of life post-transplant must be balanced by the harms introduced by lifelong immunosuppressive therapy. The Short Form health Survey 36-Item (SF-36) was administered to 69 SPK transplant recipients and 34 patients with Type 1 diabetes on hemodialysis. They also compared the transplant QoL results to a reference Spanish population. The authors attempted to control for group differences with multivariate analysis on variables of age, sex, and years duration of diabetes diagnosis. While SPK patients had lower QoL compared to the reference population across all eight domains of physical and mental well-being, they had a statistically significant higher score across these same domains in comparison to diabetic patients on dialysis. No aggregate measures were reported. Findings in a healthcare system outside the United States may not apply to U.S. populations.
 
The literature, consisting primarily of case series and registry data, demonstrate graft survival rates comparable to other solid organ transplants, as well as attendant risks associated with the immunosuppressive therapy necessary to prevent allograft rejection. No randomized controlled trials (RCTs) compare any form of pancreas transplant to insulin therapy; the PANCREAS trial (NCT01067950) is currently recruiting patients to compare isolated pancreas transplant to intensive insulin therapy in nonuremic diabetics with poorly controlled diabetes.  There was no literature identified in this policy update that would prompt a change in the coverage statement.
 
2012 Update
A search of the MEDLINE database was conducted through June 2012. There was no new literature identified that would prompt a change in the coverage statement.
 
Pancreatic transplant
Several 2011 studies addressed pancreas transplantation in individuals 50 years of age or older. A study by Afaneh and colleagues reviewed data on 17 individuals at least 50-years-old and 119 individuals younger than 50 who had a pancreas transplant at a single institution in the U.S (Afaneh, 2011). The 2 groups had similar rates of surgical complications, acute rejection and non-surgical infections. Overall patient survival was similar. Three- and 5-year survival rates were 93% and 90% in the younger group and 92% and 82% in the older group. Schenker and colleagues in Germany compared outcomes in 69 individuals at least 50-years-old and 329 individuals younger than 50 years who had received a pancreas transplant (Schenker, 2011). Mean duration of follow-up was 7.7 years. One-, 5-, and 10-year patient and graft survival rates were similar in the 2 groups. For example, the 5-year patient survival rate was 89% in both groups. The 5-year pancreas grant survival rate was 76% in the older group and 72% in the younger group. The authors of both studies, as well as the authors of a commentary accompanying the Schenker article, (Gruessner, 2011) agreed that individuals age 50 years and older are suitable candidates for pancreas transplantation.
 
Islet transplant
In 2011, Thompson and colleagues in Canada published findings from a prospective cross-over study of intensive medical therapy (pretransplant) versus islet cell transplantation in patients with type 1 diabetes (Thompson, 2011). The article reported on 45 patients; at the time of data analysis, 32 had received islet cell transplants. Eight of 45 (18%) patients were no longer being followed; 5 dropped out pretransplant and 3 post-transplant. Two were lost to follow-up, 1 withdrew after graft failure, 2 withdrew due to persistent fatigue, 2 developed malignancy, and 1 had a severe CMV infection. Primary outcome measures are HbA1c, change in glomerular filtration rate (GFR), progression of retinopathy, and change in nerve conduction velocity. Median follow-up was 47 months pre-transplant and 66 months post-transplant. The overall mean HbA1c was 7.8% pretransplant and 6.7% post-transplant; this difference was statistically significant, p<0.001. In the 16 patients for whom sufficient data pre- and post-transplant were available on renal outcomes, the median decline in GFR (mL/min/month) was -6.7 pretransplant and -1.3 post-transplant (p=0.01). Retinopathy was assessed using the International Scale which categorizes nonproliferative diabetic retinopathy as mild, moderate, or severe. Retinopathy progressed in 10 of 82 (12%) eyes pretransplant versus 0 of 51 post-transplant (p<0.01). (The numbers of patients in the retinopathy analyses was not reported). The rate of change in nerve conduction velocity did not differ significantly between groups (exact numbers not reported). The authors noted that their finding of reduced microvascular complications after islet transplantation may be due, in part, to their choice of maintenance immunosuppression. The study used a combination of tacrolimus and mycophenolate mofetil (MMF). Additional studies with larger numbers of patients are needed to confirm the impact of islet transplantation on microvascular complications and the optimal immunosuppression regimen.
 
2013 Update
A literature search conducted through June 2013 did not reveal any new information that would prompt a change in the coverage statement.
 
Pancreas Retransplant
In 2013, Buron and colleagues reported on their experience with pancreas retransplantation in France and Geneva (Buron, 2013).  Between 1976 and 2008, 568 pancreas transplants were performed at 2 centers, including 37 repeat transplants. Patient survival after a repeat pancreas transplant was 100% after 1 year and 89% after 5 years. Graft survival was 64% at 1 year and 46% at 5 years. Among the 17 patients who underwent a second transplant in a later time period i.e., between 1995 and 2007, graft survival was 71% at 1 year and 59% at 5 years. In this more recently transplanted group, graft survival rates were similar to primary pancreas transplants, which was 79% at 1 year and 69% at 5 years.
 
Allogeneic Islet Cell Transplantation
In 2008 a report was published from the Collaborative Islet Transplant Registry (CITR), which collects and monitors data on allogeneic islet transplantation in North America, Europe, and Australia, had 325 adult recipients in their registry as of April 2008 (Alejandro, 2008). Three years after first infusion, 23% of islet-alone recipients were insulin-independent (defined as insulin-independent 2 or more weeks), 29% were insulin-dependent with detectable C-peptide, 26% had lost function, and 22% had missing data. Seventy percent achieved insulin independence at least once, 71% of whom were still insulin-independent 1 year later and 52% at 2 years. Factors that favored primary outcomes were higher number of islet infusions, greater number of total islet equivalents infused, lower pretransplant HbA1c levels, processing centers related to the transplant center, and larger islet size.
 
The CITR published an updated report in 2012; the focus of the article was changes in outcomes over time (Barton, 2012). The number of patients receiving islet transplants was 214 during 1999-2002, 255 between mid-2003-2006 and 208 from 2007-2010. A total of 575 of the 677 (85%) islet transplant recipients received islets only; the remainder underwent simultaneous kidney and islet transplants. In the 1999-2002 group, rates of insulin independence were 51% after 1 year, 36% after 2 years and 27% after 3 years. Rates for the 2007-2010 group were 66%, 55% and 44%, respectively. The incidence of clinically reportable adverse events in the first year after infusion decreased from 50-53% in 1999-2006 to 38% in 2007-2010. The rates of peritoneal hemorrhage or gallbladder infusion were 5.4% in 1999-2003 and 3.1% in 2007-2010. The authors did not report findings separately for the subset of patients who underwent islet-only transplants.
 
In 2012, Vantyghem and colleagues reported on 23 patients with type 1 diabetes who underwent islet transplantation; 14 had islet-only transplants and 9 had islet after kidney transplants (Vantyghem, 2012). Median HbA1c was 8.3% at baseline and 6.7% at 3 years. Ten of the 23 patients (43%) were insulin independent 3 years after islet transplantation. Findings were not reported separately for the islet-only transplant recipients.
 
Ongoing Clinical Trials
A comparison of strict glucose control with usual care at the time of islet cell transplantation (NCT01123122) : This is a single-center randomized controlled trial (RCT) comparing the impact of strict glucose control versus usual care prior to islet cell transplantation on outcomes in patients with type 1 diabetes. The primary study outcome is islet cell function 3 months post-transplantation. The estimated enrollment is 32 patients, and the estimated study completion date is September 2015
 
A comparison of islet cell transplantation with medical therapy on the risk of progression of diabetic retinopathy and diabetic macular edema (NCT00853424) :
 This RCT is comparing islet cell transplantation to standard medical therapy in patients with diabetic eye disease. The primary outcome is progression of diabetic retinopathy or moderate visual loss. The estimated enrollment is 40 patients, and the estimated study completion date is June 2015.
 
2014 Update
 
A literature search conducted through June 2014 did not reveal any new information that would prompt a change in the coverage statement. The key identified literature is summarized below.
 
Several case series have been published. These series tend to have small sample sizes and relatively short-term follow-up. Representative series are described next.
 
In 2013, Rickels et al reported on 12 patients with type 1 diabetes and severe hypoglycemia who had islet transplantation (Rickels, 2013). Mean glycosylated hemoglobin decreased from 7.0%±0.3% before the procedure to 5.6%±0.1% after 6 to 7 months (p<0.01). All of the insulin sensitivity measures were significantly less than normal before islet transplantation and not significantly different from normal after transplantation. Adverse events were not discussed.
 
In 2013, O’Connell et al reported on 17 patients with type 1 diabetes and severe hypoglycemia who underwent islet transplantation in Australia (O’Connell, 2013). The primary end point was the proportion of patients who had had an HbA1c less than 7% and no severe hypoglycemic events 2 months after the initial transplant. (Patients could have 1 or 2 infusions.) Fourteen of the 17 (82%) patients achieved the primary end point. Nine (53%) patients attained insulin independence for a median of 26 months. At the time of data analysis for this publication, 6 patients remained insulin independent. Most adverse events related to immunosuppression. Seven of the 17 (41%) patients developed mild lymphopenia and 1 developed Clostridium difficile colitis; these all responded to treatment. Eight patients developed anemia shortly after transplant and 1 required a blood transfusion. Procedure-related complications included 1 partial portal vein thrombosis and 3 postoperative bleeds; 2 of the bleeds required transfusion. Patients were followed for different amounts of time; long-term follow-up data were not available for a consistent length of time.
 
Trial Comparing Metabolic Efficiency of Islet Graft to Intensive Insulin Therapy for Type 1 Diabetes's Treatment (TRIMECO) (NCT01148680): This randomized controlled trial is comparing islet transplantation to intensive insulin therapy in patients with type 1 diabetes. The estimated enrollment is 40 patients, and the estimated study completion date is December 2014.
 
The techniques for allogeneic islet cell transplants are evolving, and the impact on the net health outcome is still uncertain. Moreover, longer follow-up with larger numbers of patients is needed before conclusions can be drawn about the safety of allogeneic islet transplantation and its impact on diabetes mellitus and associated complications. Thus, this technology is considered investigational for patients with diabetes type 1.
  
2015 Update
 
A literature search conducted through February 2015 did not reveal any new information that would prompt a change in the coverage statement. The key identified literature is summarized below.
 
Several centers have published outcomes after pancreas retransplantation. In 2014, Seal and colleagues reported on 96 consecutive PTA patients treated at a single center in Canada; 78 were initial transplants, and 18 were retransplants (Seal, 2014). Pancreas graft survival was similar for primary transplants and retransplants at 1year (88% vs 100%, p=0.88) and 3 years (85% in both groups, p=0.99). Patient survival rates were also similar in the 2 groups at 1 year (96% and 100%, p=0.95) and 3 years (93% and 100%, p=0.93).
 
Recipient age over 50 years has in the past been considered a relative contraindication for pancreas transplant. In the past 5 to 10 years, several analyses of outcomes by patient age group have been published and there is now general agreement among experts that age should not be a contraindication; however, age-related comorbidities are important to consider when selecting patients for transplantation. In the largest study of pancreas outcomes by recipient age, Siskind and colleagues used data from the UNOS database (Siskind, 2014).Investigators included all adult patients who received SPK or PTA between 1996 and 2012 (n=20,854). There were 3160 patients between the ages of 50 and 59 years, and 280 patients age 60 or older. Overall, Kaplan-Meier survival analysis found statistically significant differences in patient survival (p<0.001) and graft survival (p<0.001) among age categories. Graft survival was lowest in the 18- to-29 age group at 1, 5, and 10 years, which the authors noted might be due to early immunological graft rejection due to more robust immune responses. However, 10 and 15 year graft survival was lowest in the 60 and older age group. Patient survival rates decreased with increasing age, and the differential between survival in older and younger ages increased with longer follow-up intervals. Lower survival rates in patients 50 and older could be due in part to comorbidities at the time of transplantation. Also, as patient age, they are more likely to die from other causes. Still, patient survival at 5 and 10 years was relatively high.
 
In 2014, the Board of Directors of the Organ Procurement and Transplantation Network issued an updated comprehensive list of transplant related policies (OPTN, 2014). Each candidate registered on the pancreas waiting list must meet one of the following requirements:
  • Be diagnosed with diabetes
  • Have pancreatic exocrine insufficiency
  • Require the procurement or transplantation of a pancreas as part of a multiple organ transplant for technical reasons
 
The policy also delineated pancreas, kidney-pancreas, and islet allocation, classifications, and rankings.
 
2018 Update
Annual policy review completed with a literature search using the MEDLINE database through March 2018. No new literature was identified that would prompt a change in the coverage statement. The key identified literature is summarized below.
 
A systematic review by Health Quality Ontario in 2015 reported on islet transplantation for patients with type 1 diabetes (Health Quality Ontario, 2015). Most of the evidence was from case series derived at single centers. For nonuremic patients, rates of insulin independence ranged from 30% to 70% from observational case series at 1 year after islet transplantation. For uremic patients, reported insulin-independence rates ranged from 20% to 67%. Evidence of changes in secondary complications such as diabetic retinopathy and nephropathy were conflicting across different studies.
 
ONGOING AND UNPUBLISHED CLINICAL TRIALS
Some currently unpublished trials that might influence this review are listed below.
 
NCT00679042  Islet Transplantation in Type 1 Diabetic Patients Using the University of Illinois at Chicago (UIC) Protocol
Expected Enrollment: 1000
Completion Date: Sep 2017
 
NCT00706420 Islet Transplantation Alone (ITA) in Patients With Difficult to Control Type I Diabetes Mellitus Using a Glucocorticoid-free Immunosuppressive Regimen
Expected Enrollment: 20
Completion Date: May 2018
 
NCT02505893 Minimal Islet Transplant at Diabetes Onset (MITO)
Expected Enrollment: 6
Completion Date: May 2018
 
NCT00160732 Allogenic Islet Cell Transplantation
Expected Enrollment: 50
Completion Date: Oct 2018
 
NCT01897688 A Phase 3 Single Center Study of Islet Transplantation in Nonuremic Diabetic Patients
Expected Enrollment: 20
Completion Date: Dec 2018
 
NCT00306098 Islet Cell Transplantation Alone in Patients With Type 1 Diabetes Mellitus: Steroid-Free Immunosuppression
Expected Enrollment: 40
Completion Date: May 2019
 
NCT01909245 Islet Cell Transplant for Type 1 Diabetes (TCD)
Expected Enrollment: 30
Completion Date: Jul 2021
 
 
NCT01974674 Allogeneic Islet Transplantation for the Treatment of Type 1 Diabetes (GRIIF)
Expected Enrollment: 19
Completion Date: Jan 2022  
 
2019 Update
Annual policy review completed with a literature search using the MEDLINE database through March 2019. No new literature was identified that would prompt a change in the coverage statement. The key identified literature is summarized below.
 
Lablanche et al published a multicenter, open-label, RCT (TRIMECO trial) evaluating patients who had type 1 diabetes with severe hypoglycemia or after kidney transplantation (Lablanche, 2018). Patients received immediate islet transplantation (n=25) or intensive insulin therapy followed by delayed islet transplantation (n=22). Median follow-up was 6 months for both groups. The primary end point was a composite score (β score) which has not been validated and which reflected fasting glucose, HbA1c level, C-peptide, and insulin independence. At 6 months, 16 of 25 patients in the immediate transplantation group and none of 22 patients in the control group had a modified β score of 6 or higher (p<0.001). Of note, few patients in the insulin group used continuous glucose monitoring or other technologies to monitor for hypoglycemia. At 6 months, insulin independence was achieved in 44% of patients in the immediate transplantation group (n=25; p<0.001). After the entire cohort received islet transplantation, the 1-year insulin independence rate was 59% (n=46; p<0.001). Subsequent to islet transplantation, 6% of patients had bleeding complications. Trial limitations included possible bias from open-label design as well as an inadequate follow-up period to demonstrate transplant durability.
 
2020 Update
A literature search was conducted through March 2020.  There was no new information identified that would prompt a change in the coverage statement.  
 
2021 Update
Annual policy review completed with a literature search using the MEDLINE database through March 2021. No new literature was identified that would prompt a change in the coverage statement. The key identified literature is summarized below.
 
There are several systematic reviews of the literature on chronic pancreatitis patients. Kempeneers et al published a systematic review of studies examining pain, endocrine function, or quality of life outcomes in patients with chronic pancreatitis undergoing total pancreatectomy with islet transplantation (Kempeneers, 2019). A total of 15 studies met the inclusion criteria. All included studies were retrospective and observational. The median age was 41 years. Pooled insulin free rate was 30% (95% confidence interval [CI], 20% to 43%) at 1 year (4 studies). The pooled mortality rate was 2% (95% CI, 1% to 4%) at 30 days (11 studies) and 4% at 1 year (6 studies). At 1 year, 63% (95% CI, 46% to 77%, I2=89%) of patients were opioid free (6 studies, 657 patients). An analysis revealed a high risk for publication bias among the included studies, which could have led to an overestimation of the true affect.
 
In 2020, the American Diabetes Association standards of medical care recommended autologous islet cell transplantation be considered in patients undergoing total pancreatectomy for chronic pancreatitis to prevent postsurgical diabetes (ADA, 2020). The standards of care note that islet cell transplantation may have a role in type 1 diabetes; however, it is considered experimental and improved blood glucose monitoring technology may be a better alternative (ADA, 2020). Because of the need for immunosuppressive agents post transplantation, the guideline notes that transplantation in type 1 diabetes should be reserved for patients also undergoing renal transplantation or experiencing recurrent ketoacidosis with severe hypoglycemia despite intensive management.
 
2022 Update
Annual policy review completed with a literature search using the MEDLINE database through March 2022. No new literature was identified that would prompt a change in the coverage statement. The key identified literature is summarized below.
 
The U.S. Food and Drug Administration (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. Allogeneic islet cells are included in these regulations. No allogeneic islet cell product is currently approved in the United States, but a biologic license application is currently under consideration by the FDA, and the Cellular, Tissue and Gene Therapies Advisory Committee voted in favor of approving the product (donislecel, purified allogeneic deceased donor pancreatic islet cells) in April 2021 (FDA, 2021; Witkowski, 2021).
 
There are several systematic reviews of the literature on chronic pancreatitis patients. Zhang et al published a systematic review and meta-analysis of 17 studies that reported clinical outcomes following total pancreatectomy with islet transplant in patients with chronic pancreatitis (Zhang, 2020). Most studies were single-center, small case series from the United States. The median age was 53 years. Insulin independence was 33.29% (95% CI, 27.77 to 39.05; I2=32.3%) at 1 year (8 studies). Mortality at 30 days was 1.32% (95% CI, 0.68 to 2.16; I2=0.0%) and mortality at 1 year was 2.54% (95% CI, 1.32 to 4.16; I2=17.6%).
 
LaBlanche et al reported 10-year outcomes from the Swiss-French GRAIL Network of 44 patients who received islet transplant for type 1 diabetes between 2003 and 2010 (Lablanche, 2021). Thirty one patients were still being followed at 10 years; 6 patients died between years 1 and 10 posttransplant. Median HbA1c levels were 7.2% (range, 6.2% to 8.0%) after 10 years compared to 8.0% pretransplant (p<.001). One patient was insulin independent at 10 years and 73.9% were free of severe hypoglycemia. Insulin requirements were significantly lower posttransplant (0.3 units/kg/day vs. 0.5 units/kg/day; p<.001). Islet graft survival was 51.9% at 10 years.
 
Two prospective, Phase 3, single-arm, open-label, multicenter trials of purified human pancreatic islet cell transplant have been conducted in North America under the guidance of the National Institutes of Health-sponsored Clinical Islet Transplantation (CIT) Consortium (Hering, 2016; Markmann, 2021). Hering et al studied 48 patients with type 1 diabetes, hypoglycemic unawareness, and a history of experiencing severe hypoglycemic events (Protocol CIT07) (Hering, 2016). The primary outcome (HbA1c level 7% and freedom from severe hypoglycemia after 1 year) was achieved in 87.5% and 71% of patients at 1 and 2 years. Median HbA1c level decreased from 7.2% at baseline to 5.6% at 1 and 2 years (both p<.001). Only 2 patients experienced severe hypoglycemia in the first year posttransplant. Insulin independence was achieved in 52.1% of patients at 1 year, and median insulin use decreased from 0.49 units/kg/day at baseline to 0 units/kg/day at 1 year (p<.0003). Glomerular filtration rate decreased posttransplant (p<.0008 vs. baseline) due to adverse effects of immunosuppression. Twenty-two serious adverse events during the first year were attributed to the procedure or subsequent immunosuppression.
 
Markmann et al conducted a similar trial in 24 patients with type 1 diabetes and hypoglycemic unawareness who had previously received a kidney transplant (Protocol CIT06) (Markmann, 2021). The primary outcome (HbA1c level 6.5% or a reduction in HbA1c level of at least 1% and freedom from severe hypoglycemia after 1 year) was achieved by 62.5% of patients. At 2 and 3 years, 58.3% and 45.8% had achieved these glycemic targets. Severe hypoglycemia was eliminated in 79.2% of patients at 1 year, 75% at 2 years, and 62.5% at 3 years. Median insulin requirements decreased from 0.5 units/kg/day at baseline to 0 units/kg/day at 1, 2, and 3 years (p<.001, p<.001, and p=.002, respectively). Kidney function remained stable throughout follow-up. Thirteen serious adverse events were considered related or possibly related to islet transplant or immunosuppression.
 
Lemos et al reported 20-year results for a retrospective series of 49 patients with type 1 diabetes, hypoglycemic unawareness, and severe hypoglycemia who underwent islet transplant (Lemos, 2021). Median follow-up time after transplant was 13.8 years. Median duration of graft function while on immunosuppression was 4.4 years (interquartile range, 1.3 to 12.2 years). Kaplan-Meier survival analysis showed cumulative survival of >80% at 20 years; 2 patients died during follow-up, 1 from myocardial infarction and 1 from suspected hypoglycemia.
 
In 2021, the American Diabetes Association standards of medical care recommended autologous islet cell transplantation be considered in patients undergoing total pancreatectomy for chronic pancreatitis to prevent postsurgical diabetes (ADA 4, 2021). The standards of care note that islet cell transplantation may have a role in type 1 diabetes; however, it is considered experimental and improved blood glucose monitoring technology may be a better alternative (ADA 9, 2021). Because of the need for immunosuppressive agents posttransplantation, the guideline notes that transplantation in type 1 diabetes should be reserved for patients also undergoing renal transplantation or experiencing recurrent ketoacidosis with severe hypoglycemia despite intensive management.
 
In 2020, the International Consensus Guidelines for Chronic Pancreatitis panel released a statement on the role of total pancreatectomy and islet transplant in patients with chronic pancreatitis (Abu-l-Haija, 2020). The panel stated that islet transplant should be considered for patients undergoing total pancreatectomy due to the potential for insulin independence and better long-term glycemic outcomes compared to pancreatectomy alone (weak recommendation based on low quality evidence). However, there is not enough information to definitively conclude when transplant should be performed relative to other interventions. Major indications for pancreatectomy with islet transplant include debilitating pain or recurrent pancreatitis episodes that diminish quality of life (strong recommendation based on low quality evidence). Contraindications to pancreatectomy with islet transplant include active alcoholism, pancreatic cancer, end-stage systemic illness, or psychiatric illness or socioeconomic status that would hinder either the procedure itself or posttransplant care (strong recommendation based on low quality evidence). Pancreatectomy with islet transplant improves quality of life, opioid use, and pancreatic pain in this population, but evidence about the effect on healthcare utilization is limited.
 
2023 Update
Annual policy review completed with a literature search using the MEDLINE database through March 2023. No new literature was identified that would prompt a change in the coverage statement. The key identified literature is summarized below.
 
In 2022, the American Diabetes Association standards of medical care recommended autologous islet cell transplantation be considered in patients undergoing total pancreatectomy for chronic pancreatitis to prevent postsurgical diabetes (Draznin, 2022). The standards of care note that islet cell transplantation may have a role in type 1 diabetes; however, it is considered experimental (Draznin, 2022). Because of the need for immunosuppressive agents posttransplantation, the guideline notes that transplantation in type 1 diabetes should be reserved for patients also undergoing renal transplantation or experiencing recurrent ketoacidosis with severe hypoglycemia despite intensive management.
 
Additional 2023 Update
In June 2023, the FDA approved donislecel-jujn for the treatment of adults with type 1 diabetes who are unable to approach target HbA1c because of repeated episodes of severe hypoglycemia despite intensive diabetes management and education (U.S. FDA, 2023). The approval was based on a phase 1/2 trial in patients with brittle type 1 diabetes complicated by hypoglycemic unawareness, metabolic lability with documented severe hypoglycemia, or ketoacidosis despite intensive insulin therapy (N=10); a single-arm, open-label phase 3 trial with similar eligibility criteria (N=20), and an expanded access protocol with similar eligibility criteria (Gangemi, 2008; Qi, 2014; ClinicalTrials.gov, 2022; ClinicalTrials.gov, 2022; U.S. FDA, 2023). In the FDA analysis of these trials (as described in the product labeling), median participant age was 46.5 years (range, 21 to 67 years); 80% of participants were female, 100% were White, and 97% were of non-Hispanic ethnicity (U.S. FDA, 2023). Patients received up to 3 islet cell infusions; among 30 participants in the approval trials, 11 received 1 islet cell infusion, 12 received 2 infusions, and 7 received 3 infusions. Twenty-five participants (83%) achieved exogenous insulin independence (defined as not requiring exogenous insulin to achieve adequate glycemic control) of any duration, including 4 patients (13.3%) with independence for less than 1 year, 12 patients (36.7%) with independence for 1 to 5 years, and 9 patients (33.3%) with independence for more than 5 years. Mean duration of exogenous insulin dependence in the phase 1/2 and phase 3 studies were 5.1 years (standard deviation [SD] 4.2, range 0.2 to 12.8) and 3.2 years (SD 3.1, range 0 to 9.9), respectively. Serious adverse reactions were reported in 90%, including 2 deaths (7%) from multiorgan failure with sepsis (1.6 years after first infusion) and progressive confusion, global atrophy, and micro-ischemic disease (9.7 years after first infusion); most serious adverse reactions were attributed to immunosuppression. Infections were reported in 26 patients (87%), totaling 211 episodes, 1 of which was classified as life-threatening and 22 as severe. Malignancy was reported in 11 subjects (37%), including 12 skin cancers and 1 each of posttransplant lymphoproliferative disease, breast cancer, and thyroid cancer. Common adverse events included, but were not limited to nausea, fatigue, anemia, diarrhea, abdominal pain, asthenia, headache, and hyponatremia. Most adverse reactions were low-grade by Common Terminology Criteria for Adverse Events, version 5; the most common grade 3 adverse events included low density lipoprotein elevations (37%), anemia (27%), and pneumonia (17%).
 
The FDA also reviewed the Clinical Islet Transplantation (CIT) consortium's phase 3, open-label, single-arm, multicenter trial (CIT-07) data (Lantrida, 2023). The trial enrolled patients with hypoglycemia unawareness and a history of severe hypoglycemic episodes. Although 8 centers participated in the trial, only the 4 patients from the single site who were treated with the particular donislecel-jujn product were included in the review. All patients received 1 or 2 islet transplants. The primary endpoint was the proportion of subjects who achieved a HbA1c less than 7% at 1 year with no hypoglycemic events from Day 28 to Day 365 after transplantation. Analysis of the primary endpoint was limited because 2 subjects had HbA1c levels less than 7% at baseline and another had near target HbA1c (7.3%). Severe hypoglycemic events were not reported. The 3 subjects who completed Day 730 follow up, were insulin independent at that time.
 
The FDA Biologics License Application Clinical Review Memorandum states numerous protocol deviations across the above studies that could impair the interpretation of both efficacy and safety data, as well as provides examples of missing and incongruent data and insufficient data monitoring during the study (Lantrida, 2023). Multiple information requests were generated by the FDA in order to achieve adequate data for a substantive, complete review. Given that the studies were conducted at a single site raises concern; and other factors that might affect occurrence or duration of insulin independence were not able to be elucidated from the existing studies, including cell product factors (number of cells, viability, purity, and potency) and delivery device (e.g., type of catheter).
 
In 2023, the American Diabetes Association standards of medical care recommended autologous islet cell transplantation be considered in patients undergoing total pancreatectomy for chronic pancreatitis to prevent postsurgical diabetes (ElSayed, 2023). The standards of care note that islet cell transplantation may have a role in type 1 diabetes. Because of the need for immunosuppressive agents posttransplantation, the guidelines note that transplantation in type 1 diabetes should be reserved for patients also undergoing renal transplantation or experiencing recurrent ketoacidosis with severe hypoglycemia despite intensive management.
 
2024 Update
Annual policy review completed with a literature search using the MEDLINE database through March 2024. No new literature was identified that would prompt a change in the coverage statement.
 
Additional 2024 Update
Annual policy review completed with a literature search using the MEDLINE database through September 2024. No new literature was identified that would prompt a change in the coverage statement. The key identified literature is summarized below.
 
In 2024, the American Diabetes Association (ADA) standards of medical care recommended autologous islet cell transplantation be considered in patients undergoing total pancreatectomy for chronic pancreatitis to prevent postsurgical diabetes (ElSayed, 2024). The standards of care note that islet cell transplantation may have a role in type 1 diabetes. Because of the need for immunosuppressive agents posttransplantation, the guidelines note that transplantation in type 1 diabetes should be reserved for patients also undergoing renal transplantation or experiencing recurrent ketoacidosis with severe hypoglycemia despite intensive management. The ADA also states that 'In much of the world, allogenic islet transplantation is regulated as an organ transplant. However, in the U.S., allogenic islet transplantation is regulated as a cell therapy, and the first such allogeneic islet cell therapy, donislecel-jujn, was approved in 2023. Donislecel is indicated for the treatment of adults with type 1 diabetes who are unable to approach their A1C goal because of current repeated episodes of severe hypoglycemia despite intensive diabetes management and education.' However, no recommendation was provided for the use of allogenic islet transplantation.

CPT/HCPCS:
0584TIslet cell transplant, includes portal vein catheterization and infusion, including all imaging, including guidance, and radiological supervision and interpretation, when performed; percutaneous
0585TIslet cell transplant, includes portal vein catheterization and infusion, including all imaging, including guidance, and radiological supervision and interpretation, when performed; laparoscopic
0586TIslet cell transplant, includes portal vein catheterization and infusion, including all imaging, including guidance, and radiological supervision and interpretation, when performed; open
48160Pancreatectomy, total or subtotal, with autologous transplantation of pancreas or pancreatic islet cells
G0341Percutaneous islet cell transplant, includes portal vein catheterization and infusion
G0342Laparoscopy for islet cell transplant, includes portal vein catheterization and infusion
G0343Laparotomy for islet cell transplant, includes portal vein catheterization and infusion

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