Frequently Asked Questions

Common questions about the transplant process, waitlists, and how to use transplant.today.

Can I list at multiple transplant centers?

Yes. OPTN policy permits registering at more than one transplant hospital at the same time, which is called multiple listing. Each program evaluates you separately and you hold a separate registration at each.

Two things worth knowing about your rights here. Programs are required to tell you at evaluation that multiple listing is an option, so if nobody has mentioned it, ask. At the same time, an individual program is allowed to decline to register you specifically because you are listed elsewhere, so it is not guaranteed that any center you approach will take you. New York State separately restricts kidney multiple listing for candidates listed in state.

The practical barriers are real: a second full evaluation that insurance often will not cover twice, travel costs, and the requirement that you can reach the second hospital quickly when it calls. See does a second listing actually help for what it buys you.

Does listing at a second center actually help for deceased-donor organs?

It can, but the reason is commonly misunderstood, including in earlier versions of this page.

The misconception. It is natural to picture each center as fishing in its own local donor pool, so that a second listing buys you a ticket in a second lottery. That is not how allocation works. Every deceased-donor organ generates one national match run that already includes every compatible candidate in the country. You are never excluded from a distant donor because of where you are listed.

What actually happens. Distance is a scoring factor inside that one national list, not a gate. Being listed at a second hospital gives you a second, independently scored entry in every match run, with distance measured from that second hospital. For a donor near the second center, that entry can rank far higher than your first entry does. So a second listing improves your rank on certain match runs rather than granting access to runs you were shut out of.

Two consequences follow from that:

  • Distance between the two centers is what matters. The benefit is concentrated in the area around the second center that your first center's circle does not already cover. Two programs in the same metro area have nearly identical proximity scoring, so a second listing there adds very little. OPTN's own patient guidance says as much.
  • The second program's behavior may matter as much as its location. A center that accepts organs your first center declines converts more of your rankings into an actual transplant. Center acceptance rates vary widely, and SRTR publishes a risk-adjusted offer acceptance rate ratio per program that you can look up.

Kidney is the strongest case, because kidney waiting time follows a clinical milestone rather than a listing date, so a second kidney listing starts with all your accrued time rather than from zero. For liver, heart, and lung, the new clock starts at listing, though urgency scoring matters more than accrued time for those organs anyway.

The evidence, and its caveat. Registry studies going back to 2004 consistently find multi-listed candidates are transplanted at higher rates. But multi-listed patients are also more likely to be white, college-educated, and privately insured, so a good part of the measured advantage reflects who can afford a second evaluation and the travel it requires rather than the listing itself. OPTN's own ethics committee has examined multiple listing on exactly these grounds: the option is formally open to everyone and practically available mainly to people with resources.

What our tools do and do not do. The simulator estimates your probability at each center independently. It does not combine two centers into a single joint probability, so treat two center estimates as two separate figures rather than adding them. Your combined odds are better than either alone, but by less than the sum, since the two registrations compete for many of the same organs.

Sources: OPTN patient guidance on multiple listing, Merion et al. 2004, Giorgakis et al. 2025, SRTR offer acceptance rate ratio.

How does blood type affect my wait time?

Blood type affects allocation because donors and recipients have to be compatible, which changes the size of the donor pool available to you:

  • Type O can receive only from type O donors, and waits longest for a kidney
  • Type A can receive from types A and O
  • Type B can receive from types B and O, and often waits longer because there are fewer type B donors
  • Type AB can receive from any blood type and generally waits the least

There is one important exception that is easy to miss. Since the kidney allocation system changed in December 2014, type B candidates can also accept kidneys from certain A and AB donors whose subtype is A2 (also written non-A1 and non-A1B). These organs behave like type O for a type B recipient, and taking them can meaningfully shorten a type B candidate's wait. The catch is that offering this is a program decision, not an automatic one: OPTN has reported that the large majority of transplant programs perform none of these transplants at all. If you are type B, ask your program directly whether it accepts A2 and A2B kidneys, because a program that does not is leaving that shortcut unused. See what does my transplant program decide.

transplant.today incorporates blood type into its Monte Carlo simulation to estimate personalized wait time probabilities.

What does "as expected" mean on SRTR reports?

"As expected" is a risk-adjusted performance rating from SRTR. It means the center's outcomes (like graft survival) are statistically consistent with what would be predicted given the complexity of patients they treat.

SRTR adjusts for factors like patient age, diagnosis, and comorbidities, so a center treating sicker patients isn't penalized. The three ratings are:

  • Better than expected: outcomes significantly above the risk-adjusted prediction
  • As expected: outcomes within the normal statistical range
  • Worse than expected: outcomes significantly below the prediction

Most centers are rated "as expected." A rating of "worse than expected" triggers additional CMS oversight.

How are organs allocated in the United States?

Deceased-donor allocation works in two layers, and it is worth keeping them separate because they are governed by different people.

The national layer. Each time a deceased donor's organs become available, UNOS runs one computerized "match run" for that donor under OPTN policy. It produces a ranked list of candidates. The ranking depends on:

  • Medical urgency, scored differently for each organ (MELD for liver, status tiers for heart, the Composite Allocation Score for lung)
  • Blood type compatibility, which is required
  • Tissue typing and sensitization (cPRA), which matter most for kidney
  • Accrued waiting time, which weighs most heavily for kidney
  • Distance from the donor hospital, measured in nautical miles rather than by state or region
  • Pediatric priority and prior living donor priority

The program layer. Your transplant program decides whether to list you at all, and whether to accept each organ it is offered on your behalf. Those decisions belong to the program rather than to OPTN policy, and they differ substantially between centers. See what does my transplant program decide below.

Learn more on our Education page or at unos.org.

What does my transplant program decide, and what does the national system decide?

The national system decides the order in which candidates are offered a particular deceased-donor organ. Your program decides almost everything around that order, and those decisions are where much of the difference between centers comes from.

Set by OPTN policy, identical everywhere: the ranking logic of the match run for each deceased donor. A program cannot move its own patient up the list.

Decided by your program:

  • Whether to list you. Federal regulation (42 CFR 482.90) requires each program to use written patient selection criteria and to document which criteria it applied to you. It does not tell programs what those criteria should be. Age limits, BMI thresholds, sobriety periods, psychosocial requirements, and caregiver-support requirements are set center by center and vary widely.
  • Whether to accept an offer for you. When the match run reaches your name, your program decides accept or decline, usually within about an hour, and often without contacting you.
  • Which kinds of organs it is willing to use, such as higher-KDPI kidneys, donation after circulatory death, hepatitis C positive donors, or A2 and A2B kidneys for type B candidates.
  • Whether to request an urgency status exception for you, for heart, liver, and lung. The requested upgrade takes effect immediately and is reviewed by a regional or national review board afterward, so how aggressively your center files exceptions affects your priority.
  • Which of its own patients gets the organ, in the specific pathways described in the next question.

One practical note. Programs must give you a copy of their written selection criteria if you ask, but they are not required to publish them. A 2025 review of 255 US kidney program websites found only about 2.6 percent of the selection-criteria items that guidelines recommend disclosing were actually posted online. Ask your coordinator for the written criteria rather than assuming the website is complete.

Sources: 42 CFR 482 subpart E, JMIR AI 2025 transparency study, OPTN review boards.

Can my transplant program choose which of its own patients gets an organ?

Yes, in specific situations. Most of the time the match run sets the order and the program only accepts or declines. But there are pathways where the program itself selects the recipient from among its own listed candidates, which means two programs with identical waiting lists could genuinely choose different people.

Non-directed living donors. When someone donates a kidney without a specific recipient in mind, no deceased-donor match run applies, because the national algorithm is built around deceased-donor characteristics. The program decides which of its candidates receives that kidney, or enters the donor into a paired-exchange chain. OPTN policy explicitly leaves the choice of who receives a chain-ending kidney to the transplant hospital. How the program weighs time waiting against medical urgency, expected benefit, or degree of sensitization is its own judgment, made through its selection committee. Note that most US paired exchange runs through private registries such as the National Kidney Registry and the Alliance for Paired Kidney Donation rather than OPTN's own smaller program, and their rules differ, so ask which registry your center uses.

Allocation out of sequence. When an organ is at risk of not being placed, because many centers have declined it or because time and logistics threaten its viability, it may be placed outside the strict match-run order. The organ procurement organization approaches a center directly, and the accepting center then chooses which of its own candidates receives it.

This practice grew quickly, from about 2.3 percent of deceased-donor kidney placements in 2020 to roughly 16 percent by 2023, and it varied enormously between organ procurement organizations, from none at all to more than 40 percent. That growth drew serious criticism, because recipients of these organs skew toward patients who are older, male, and privately insured, while candidates who are highly sensitized or pediatric can be passed over.

This area is actively changing right now. In February 2025 HRSA directed the OPTN that the governing federal regulations do not actually authorize out-of-sequence offers as they had been practiced, and told the OPTN to build formal expedited-placement policy instead. Draft proposals went to HRSA and the OPTN board in January 2026 and were still under review as of August 2026. If you are reading this to understand current rules, check the OPTN site rather than relying on this paragraph. One narrower pathway, expedited liver placement, has been settled policy since March 2021.

So if your ethics course framed this as a committee deciding how to prioritize among a program's existing candidates for an available organ, that describes real pathways rather than a hypothetical.

Sources: OPTN allocation out of sequence, HRSA directive, February 2025, prevalence of out-of-sequence kidney allocation, chain-end allocation study.

Who oversees the decisions my program makes about me?

Oversight is real but it is mostly internal to the program, which surprises many patients.

The selection committee. Listing decisions are made by a multidisciplinary committee, typically surgeons, physicians, coordinators, social workers, dietitians, and often a psychologist or psychiatrist. Programs are expected to have a defined, documented selection process, but no federal rule prescribes who sits on the committee or how it votes, and published reviews describe committee practice as varying considerably between centers.

Hospital ethics committees. Many programs bring difficult cases to an institutional ethics committee, and this is where the ethics oversight taught in medical school lives. It is standard practice rather than a federal requirement for individual candidate selection.

The independent living donor advocate. For living donation there is a specific mandated safeguard. Every program doing living-donor transplants must provide an independent living donor advocate, required by 42 CFR 482.98(d) and by OPTN policy. The advocate represents the donor's interests, not the recipient's or the program's, must be knowledgeable about living donation, medical ethics, and informed consent, and must not be routinely involved in the program's transplant activities. Prospective donors have to be told who this person is and how to reach them.

Above all of it, OPTN itself. Worth knowing that OPTN governance is currently mid-restructuring. Since 2023 the federal government has been breaking the single long-standing contractor model into multiple contractors, and an independent 34-member OPTN board was announced in June 2025. Allocation rules are being made by a structure still in transition.

Sources: 42 CFR 482.98, review of selection committee ethics, HRSA OPTN modernization updates.

Why do two centers with similar patients get different results?

Largely because they make different decisions about which organs to accept. This is one of the better-measured effects in transplant research.

For heart transplant, after adjusting for donor, recipient, and geographic differences, centers varied from about 12 percent to about 62 percent in how often they accepted the first organ they were offered for a candidate. Each 10 percent increase in a center's adjusted acceptance rate was associated with roughly a 27 percent lower risk of dying on the waitlist. Candidates at the most conservative centers had the highest waitlist mortality.

The part that matters most: organs accepted at first rank showed no worse five-year survival or graft failure than organs accepted further down the list. Declining aggressively did not buy better outcomes for the patients who eventually got transplanted. It mostly meant longer waits and more deaths before transplant.

Acceptance behavior also varies by patient. One analysis found Black heart candidates were about 24 percent less likely than white candidates to have a first offer accepted on their behalf, with smaller gaps for liver and lung. Because the national score does not account for what a center does with an offer, this kind of variation compounds rather than corrects existing disadvantage.

This is worth asking your program about directly. Reasonable questions: what fraction of offers do you accept for patients like me, will you use higher-KDPI or DCD or hepatitis C positive donors, and how quickly would you expect to accept something for me.

Sources: JAMA Cardiology on center offer acceptance, racial gaps in offer acceptance.

What is the difference between graft survival and patient survival?

These are two distinct measures of transplant success:

  • Graft survival: the transplanted organ is still functioning. If the graft fails, the patient may return to the waitlist or go on dialysis (for kidneys).
  • Patient survival: the patient is alive, regardless of whether the transplanted organ is still working.

Patient survival is usually higher than graft survival because a patient can survive graft failure (e.g., return to dialysis). Both metrics are shown on our Center Explorer detail pages.

How often is transplant.today data updated?

transplant.today uses automated data pipelines that refresh from public sources:

  • Weekly: EPA air quality, CDC health demographics, CMS hospital quality, BLS cost of living
  • Bimonthly: SRTR transplant center data (released semi-annually by SRTR)
  • Live: Center contact info is fetched from SRTR in real-time when you view a center detail page

Each data source shows its last-updated date on the freshness banner in the simulator.

Do I lose my accrued waiting time if I add or switch centers?

It depends on the organ, and the difference is bigger than most patients expect.

Kidney: your time is not tied to a center at all. Kidney waiting time starts at the earlier of the day you began regular dialysis or the day a documented eGFR or creatinine clearance of 20 mL/min or less was recorded. That is a clinical milestone, not a registration date, so any kidney program calculating your qualifying date arrives at the same answer. Adding a second center does not reset your clock. Since July 27, 2022, this calculation is race-neutral, and candidates whose earlier eGFR values were adjusted for race can have waiting time restored.

Liver, heart, lung, and intestine: the clock is per program. Waiting time at each hospital starts on the day that hospital listed you, so a new listing starts a new clock there. This matters less than it sounds, because for these organs medical urgency (MELD or PELD, status tier, Composite Allocation Score) drives allocation far more than accrued time does.

Separately from adding a center, you can formally request that your primary waiting time transfer between programs when you move your care. Both programs have to agree. Ask the coordinators at both centers to start this, and confirm in writing that it went through before you rely on it.

What happens if I become too sick for transplant?

If your health deteriorates significantly, the transplant team may make your listing inactive (older documents call this Status 7) or remove you from the waitlist. This can happen if:

  • You develop an active infection
  • A new cancer diagnosis requires treatment first
  • Your overall condition makes surgery too risky

Going inactive is not the same as being removed. Kidney candidates keep accruing waiting time while inactive, and once the issue resolves your team can reactivate the listing. But an inactive listing receives no organ offers, so the accruing time only pays off if you actually get reactivated, and studies of the kidney waitlist have found that many candidates listed as inactive never are. It is reasonable to ask your team directly what has to change for you to become active again, and to keep asking. The "Removed (too ill)" statistic on our center pages reflects candidates who came off the list entirely.

How does geographic distance affect organ offers?

Distance is measured in nautical miles from the donor hospital to the hospital where you are listed. Donation Service Areas and UNOS regions, the older fixed boundaries, have been removed from allocation. The details differ by organ:

  • Kidney and pancreas (since March 15, 2021): candidates within a 250 nautical mile circle around the donor hospital are considered first. Inside that circle you earn up to 2 proximity points, scaling down to zero at the edge. If the organ travels further, candidates outside the circle can earn up to 4 proximity points, scaling down out to 2,500 nautical miles.
  • Liver and intestine (since February 4, 2020): "acuity circles" of 150, 250, and 500 nautical miles, entered in an order that depends on MELD or PELD score and Status 1 urgency.
  • Lung (since March 9, 2023): distance is one weighted component of the Composite Allocation Score rather than a separate circle step. Its weight was raised from 10 to 15 points after the initial rollout.
  • Heart: urgency status tiers, each offered within 250 nautical miles before widening.

Because distance is measured to your listing hospital, where you are listed changes which match runs you appear on. Centers drawing on areas with more donors relative to demand tend to have shorter waits. transplant.today factors donor supply and allocation distance into its scoring.

OPTN is gradually replacing circles with "continuous distribution," a single weighted score. Lung has moved; kidney, liver, and heart are still in development as of August 2026.

What are cPRA, MELD, and CAS scores?

These are the organ-specific clinical scores used in allocation:

  • cPRA (calculated panel reactive antibody), kidney. Measures how sensitized you are to donor antigens. A higher cPRA, on a 0 to 100 percent scale, means fewer compatible donors, so highly sensitized candidates earn priority points to offset that.
  • MELD (Model for End-Stage Liver Disease), liver. Predicts short-term mortality without transplant from lab values including bilirubin, INR, creatinine, and sodium. Scores run from 6 to 40, and a higher score means more priority.
  • CAS (Composite Allocation Score), lung. Replaced the Lung Allocation Score on March 9, 2023. Rather than a single urgency-versus-benefit score, CAS adds up weighted points across medical urgency, expected post-transplant survival, biological disadvantage such as blood type and height, placement efficiency (distance), pediatric priority, and prior living donor status. The weights have already been revised once since 2023, so check the OPTN CAS calculator for the current table.

Heart uses urgency status tiers rather than a single composite score.

transplant.today lets you enter these scores in the simulator for more personalized wait time estimates. One caveat we want to be upfront about: the simulator now accepts your CAS score and converts it to the model's LAS-era scale through a documented statistical mapping (quantile matching of the two score distributions); the underlying multiplier tables remain LAS-era, which we track as a known limitation. Learn more on our Education page.

Have more questions? Check our Education page for detailed guides, browse Organ Guides for organ-specific information, explore Patient Support resources, or use our Find My Centers tool to get started.