Tuesday, October 20, 2026

Katherine Screws Waited Three Years for a Transplant. What If Healthcare Is Solving the Wrong Problem?

A patient’s search for answers reveals an uncomfortable truth about complex systems: when information is fragmented, people can follow the process and still get stuck. From transplant care to medical billing, are we fixing problems—or simply getting better at cleaning up the mess?

 


“Whatever the organ, most patients don’t know what to ask,” said Dr. Allyson Hart, a researcher at Hennepin Healthcare Research Institute, in Associated Press

 

It is a simple observation with a much bigger implication.

What happens when people must navigate a complicated system without understanding how it works, which options are available, or what is standing in their way?

Sometimes, the problem is not a lack of effort.

Sometimes, it is not a lack of expertise.

And sometimes, it is not even a lack of technology.

Sometimes, people simply cannot see the information they need to make their next move.

That is the question raised by the experience of Katherine Screws, a Phoenix woman whose three-year wait for an intestine transplant illustrates the human consequences of navigating a complicated healthcare system.

Her story also raises a question for physician-owned practices: How much administrative frustration could be avoided if the right information became visible before the next step went wrong?

Because healthcare has an impressive collection of software, portals, databases, dashboards, and artificial intelligence.

Yet somehow, people still end up asking the digital equivalent of, “Has anyone seen the paperwork?”

Apparently, the paperwork has achieved interoperability with everyone except the person who needs it.


A six-month expectation became a three-year wait

In May 2022, one month after marrying her husband, Stephen Gerrish, Katherine Screws was involved in a car crash that destroyed her small intestine.

She could no longer absorb nutrition normally. She depended on overnight intravenous nutrition, often felt too sick to get out of bed, and could not return to her engineering career or pursue her plans to start a family.

She had been told that a transplant might be possible within approximately six months.

Instead, she waited three years.

During that time, Screws faced more than a medical challenge. She was trying to understand a system whose options, processes, and decisions were not always clear to her.

The turning point came when she connected with Lisa Stocks, a nurse at California's organ procurement organization, OneLegacy.

Stocks helped Screws understand that transplant centers can differ in their practices and in which donor organs they are willing and able to accept. Screws also learned about publicly available information that could help her compare transplant centers.

She explored the Scientific Registry of Transplant Recipients database and registered at MedStar Georgetown University Hospital in Washington, D.C., in addition to her original center, UCLA Health.

In June 2025, just weeks after registering at Georgetown, she received her intestine transplant.

Dr. Cal Matsumoto, a transplant surgeon at MedStar Georgetown University Hospital, and his team performed the procedure. The donor intestine was longer than usual, but it fit successfully.

The story also features Dr. Syed Ali Husain of NYU Langone Health, who researches differences in transplant practices, and Dr. Allyson Hart, who helped develop patient-friendly tools for comparing transplant centers.

UCLA Health declined to comment on Screws's individual care, citing patient privacy rules, but said it follows federal transplant guidelines and continually strives to improve its processes.

Screws was careful to explain that her frustration was not simply directed at her original physicians. She was troubled by the lack of clear, centralized information about what to expect and what might be holding up progress.

Her experience does not prove that every transplant delay is avoidable or that one hospital's decisions are inherently better than another's. Transplantation involves difficult clinical judgments, complex logistics, and time-sensitive matching.

But it does demonstrate the importance of understanding how a system works and knowing what questions to ask.

The most important question may not be, “Why is this taking so long?” It may be, “What is actually holding this up—and what can I do about it?”

That question belongs in many more places across healthcare.


The contrarian argument: Maybe healthcare doesn't need another dashboard

When something goes wrong, the instinct is often to add something.

Another application. Another workflow. Another reporting tool. Another automated notification. Another dashboard showing that the other dashboard has a problem.

Before long, the organization has a dashboard for the dashboard.

But what if the underlying problem is not always the absence of a tool?

What if the information already exists somewhere—but is incomplete, disconnected, outdated, difficult to interpret, or unavailable to the person who needs it?

Consider how a medical practice operates.

The physician understands the patient's clinical circumstances. The front office manages registration. The authorization team works with payer requirements. The scheduler coordinates appointments. The medical biller needs the documentation and information required to submit an accurate claim.

Each person may be doing their job correctly.

Yet the overall process can still fail if important information does not reach the next person at the right time.

A patient's coverage may have changed. A referral may be missing. An authorization may still be pending. A documentation requirement may not have been identified until after the encounter.

The practice discovers the problem later, when correcting it is more expensive and disruptive.

This is the distinction between optimizing a task and improving the system that connects the tasks.

A faster process can still be a bad process. An automated error is still an error. And an AI-generated answer cannot make missing information magically appear.

Technology can improve healthcare enormously. But adding technology without addressing the quality and continuity of information may simply help an organization process its existing problems more efficiently.

That is progress of a sort.

It is just not necessarily the progress we need most.


What Katherine's experience can teach us—and what it cannot

An intestine transplant and a rejected medical claim are not equivalent.

The medical stakes, ethical considerations, clinical decisions, and consequences are fundamentally different. Katherine's story should not be used to suggest that a billing platform could have shortened her transplant wait, nor should it be interpreted as an accusation of negligence against the professionals involved.

The connection is more specific.

People need understandable, timely information to navigate complex systems and make informed decisions.

For a transplant patient, that may mean understanding how centers differ, which options are available, and what questions to discuss with a transplant team.

For a physician-owned practice, it may mean knowing whether a referral is complete, whether authorization is confirmed, whether coverage information is current, and whether documentation supports the service being billed.

Different situations. Different stakes. A shared challenge: information must be available and understandable before it can guide action.

In both settings, the existence of a process does not guarantee that the people navigating it can see how it works.

That is why information transparency matters.


The hidden cost of discovering problems too late

Imagine a physician evaluating a patient and determining that a procedure is medically appropriate.

The appointment is scheduled. The clinical note is written. The patient expects the next step to happen.

But several administrative questions remain:

  • Is the insurance information current?
  • Does the patient's plan cover the service under the applicable conditions?
  • Is prior authorization required?
  • Is a referral necessary?
  • Does the documentation contain the information required to support the request?
  • Has the authorization status reached the scheduling team?
  • Will the eventual claim accurately reflect the service provided and documented?

These questions may involve different staff members, systems, and payer requirements.

If one requirement is missed, the problem might not become visible until the procedure is scheduled, the service is performed, or the claim is submitted.

Then the practice must investigate.

Someone retrieves the documentation. Someone contacts the payer. Someone follows up on the authorization. Someone corrects the claim. Someone explains the delay to the patient. Someone tries to determine why the process failed.

And the physician may be asked to clarify a note weeks after the encounter.

The organization has now paid for the work twice: once to perform the original task and again to repair the process.

This is where administrative friction becomes a financial and operational problem.

A denied claim is not just a line in a report. It can represent staff time, delayed reimbursement, additional patient communication, and work that could have been directed elsewhere.

The critical question is not merely, “How do we fix this claim?”

It is:

“What happened before the claim that made this problem possible?”

That is the upstream question.


The prior authorization problem is not just paperwork

The American Medical Association's prior authorization research has documented substantial administrative burdens for physicians and patients.

Its 2025 physician survey, reported in 2026, found that:

  • 95% of surveyed physicians said prior authorization delays access to necessary care.
  • 92% said it negatively affects clinical outcomes.
  • 79% said patients abandon treatment because of authorization challenges.
  • 94% said prior authorization contributes to physician burnout.
  • Physicians and staff reported spending an average of 13 hours per week dealing with prior authorization.

These are survey findings, not proof that every delay causes harm or that one technology solution can eliminate the burden. But they illustrate how much effort the process can consume.

For a small practice, 13 hours a week is substantial.

That time has to come from somewhere: patient communication, referral coordination, follow-up, documentation, or other work that also matters.

And the irony is hard to miss. Healthcare continues to invest in digital transformation while physicians and staff spend hours navigating administrative requirements across fragmented systems.

We have digitized many processes.

We have not necessarily connected them.


Three lessons from the people in Katherine's story

1. Katherine Screws: People cannot act on options they cannot see

Screws's experience shows why accessible information matters.

For practices, the equivalent question is whether each authorized team member can see the information needed to move work forward.

Can the scheduler see that authorization is pending?

Can the physician understand which documentation requirement remains unresolved?

Can the biller distinguish a genuine coding question from an eligibility issue?

Can the practice owner identify recurring problems without manually reconstructing events from multiple systems?

The answer is not to give everyone unrestricted access to everything. Privacy, security, and role-based access are essential.

The objective is to make relevant information available to the right person at the right time.

2. Lisa Stocks: Experience is valuable—but it should not live only in someone's memory

Stocks helped Screws understand the transplant system and explore additional options.

Medical practices also depend on people with experience. A skilled biller may know that a particular payer repeatedly requests certain documentation. A referral coordinator may understand which records a specialist requires. A front-office employee may recognize a recurring eligibility problem.

That knowledge is valuable.

But if it exists only in someone's memory, a personal spreadsheet, or an old email thread, the organization cannot reliably apply it across future encounters.

The solution is not to replace experienced employees.

It is to preserve useful knowledge, make recurring requirements visible, and reduce dependence on memory alone.

Even an outstanding employee cannot simultaneously be the practice's database, notification system, and institutional memory.

3. Dr. Syed Ali Husain, Dr. Allyson Hart, and Dr. Cal Matsumoto: Context changes how information should be interpreted

The transplant reporting describes differences among centers and the clinical judgment involved in evaluating donor organs.

That reinforces a broader principle: A decision cannot be understood simply by looking at its outcome without considering the circumstances behind it.

The same is true of medical billing.

A denial does not automatically mean a coder made a mistake. A missing authorization does not necessarily mean a scheduler was careless. A documentation gap does not automatically mean a physician failed to provide appropriate care.

The cause could involve changing payer requirements, incomplete registration, a communication breakdown, a documentation issue, or a process that failed to make an important requirement visible.

Counting failures tells us what happened. Understanding their causes tells us what to change.

That is the difference between reporting a problem and learning from it.


The myth: More AI automatically means less administrative work

AI can help identify patterns, summarize information, flag potential inconsistencies, and support routine tasks.

But AI is not a substitute for good data, appropriate clinical judgment, or a well-designed process.

Imagine an automated system submitting an authorization request with incomplete information. It can submit the request quickly, but the payer may still return it for missing details.

Imagine an AI tool generating a polished clinical note that omits a fact necessary to explain the service. The language may sound excellent while the underlying problem remains.

Imagine a denial-management platform that helps staff categorize rejected claims. That may be valuable, but categorizing the same recurring problem does not necessarily prevent it from happening again.

None of these tools is inherently bad. Each may address part of the problem.

The mistake is assuming that automating one step automatically improves the entire process.

In a September 30, 2026, joint statement, six major physician organizations—including the American Medical Association, the American College of Physicians, and the American College of Surgeons—warned against treating AI as a replacement for physician expertise. They emphasized that clinical context, professional judgment, patient safety, and accountability must guide the development and use of AI.


The lesson for healthcare administration is equally important: Technology should support better decisions, not simply accelerate activity.

Before adopting an AI tool, ask:

  • Does it help identify the underlying issue?
  • Does it use reliable, relevant information?
  • Does it explain what remains unresolved?
  • Does it help the appropriate person take the next step?
  • Can the practice audit its outputs and correct mistakes?
  • Does it preserve human oversight where judgment is required?

If the tool only makes the existing queue move faster, it may still be useful. But it is solving a different problem from preventing avoidable work.


What upstream billing intelligence looks like in practice

Upstream billing intelligence starts with the idea that many preventable billing problems have contributing conditions that exist before a claim is submitted.

Those conditions can arise during registration, eligibility verification, scheduling, referral management, authorization, documentation, coding, or charge capture.

A practical framework is:

Capture → Structure → Preserve → Propagate → Act → Learn

Capture: Collect relevant information when it becomes available.

Structure: Organize it so people and systems can interpret it consistently.

Preserve: Retain the context behind important decisions, requirements, and exceptions.

Propagate: Make the information available to authorized people and downstream systems that need it.

Act: Flag unresolved requirements and help the responsible person determine the next appropriate step.

Learn: Analyze recurring patterns and improve the process based on evidence.

For example, if a procedure requires authorization, the practice should be able to distinguish an authorization that is requested from one that is approved or confirmed as unnecessary.

If documentation appears to be missing a required element, the system should flag the issue for appropriate review rather than silently assuming the record is complete.

If a payer repeatedly requests the same information, the practice should investigate whether a template, training, handoff, or process needs improvement.

This does not mean every denial can be prevented. Some result from payer decisions, clinical disagreements, changing rules, or circumstances outside the practice's control.

It means the practice should identify and address the preventable conditions it can influence.

The best time to discover a missing requirement is generally before additional work depends on it.


Seven metrics that reveal whether the process is improving

A practice does not need 47 dashboard widgets to start making progress. It needs a few consistent measures that lead to useful decisions.

  1. First-pass claim acceptance: How often do claims pass initial submission checks without preventable errors? Distinguish clearinghouse acceptance from payer adjudication.
  2. Denial rate by root cause: Separate authorization, eligibility, coding, documentation, and other relevant causes rather than relying only on the overall rate.
  3. Rework hours: Measure staff time spent correcting preventable errors, retrieving information, and resubmitting claims.
  4. Authorization lead time: Track the time required to move from a complete request to a documented decision, separating payer delays from internal delays.
  5. Missing-information rate: Measure how often work reaches a critical step without the information required to proceed.
  6. Repeat-error rate: Determine how frequently the same underlying problem recurs after it has been addressed.
  7. Patient-impact indicators: Where appropriate, monitor avoidable rescheduling, care delays, unexpected financial communications, and related outcomes.

Establish a baseline, define each measure consistently, and review the results regularly.

The goal is not to make the dashboard prettier.

It is to answer a more important question:

Are we preventing more problems—or merely getting better at cleaning them up?


A four-week experiment for a small medical practice

Improving a process does not necessarily require purchasing a new platform.

Start with one recurring problem.

Week 1: Find the pattern.

Review a sample of recent denials, authorization delays, or claim corrections. Identify where the issue first appeared.

Week 2: Map the information.

Determine where the required information originates, who verifies it, where it is stored, who needs it next, and how the current process fails.

Week 3: Test one change.

Try a targeted checklist, a standardized field, a clearer handoff, or an appropriate alert. Avoid adding steps that do not address a defined problem.

Week 4: Measure the result.

Compare the results with the baseline. Review error frequency, rework hours, delays, and staff feedback. Check for unintended consequences.

If the change helps, refine it. If it does not, investigate why before automating it.

This is not the most glamorous AI demonstration. Nobody is going to make a viral video about a missing authorization field that was completed correctly the first time.

But that is precisely the point.

A problem prevented is often less visible than a problem repaired.

It is also frequently less expensive to deal with.


Where OnnX 2.0 fits

This is the problem OnnX 2.0 is being developed to address.

OnnX is an upstream intelligence platform for healthcare, built by physicians and medical billers to reduce downstream administrative and billing noise so physicians can focus on clinical care.

Built by physicians and medical billers since 1995, the OnnX 2.0 concept focuses on the information and decisions that influence billing before a claim becomes a problem.

Clinical context, patient information, coverage, authorization requirements, referrals, documentation, and operational decisions can become fragmented across people and systems.

When the relevant information does not travel with the work, downstream teams must reconstruct it.

OnnX 2.0 is being developed around a different approach: make important context more structured, visible, and actionable so physician-owned practices can recognize information gaps earlier and investigate risks before they become avoidable rework.

The objective is not to promise zero denials or claim that every billing problem can be eliminated. It is to focus on upstream causes that a practice may be able to identify and address.

That means asking different questions.

Instead of only asking how to process a denial faster, ask what created the conditions for it.

Instead of only asking how to chase missing information, ask why it was missing when it was needed.

Instead of buying another dashboard, ask which decision the dashboard should help someone make.

The aim is to move from reactive billing toward more predictable, informed revenue-cycle operations.

That is a development vision, not a claim that every capability has already been validated in practice. The value must ultimately be demonstrated through real workflows, measurable results, and appropriate safeguards.

But the principle is worth pursuing: Better information upstream can create better opportunities to prevent problems downstream.


The future of healthcare may depend on what we stop having to fix

Katherine Screws's experience reminds us that navigating a complicated system can be difficult even when the people inside it are working hard.

Her story does not prove that every delay is avoidable. It does show why accessible information, clear explanations, and an understanding of available options matter.

For physician-owned practices, the parallel is not the severity of the outcome. It is the importance of visibility and informed action.

A patient should not have to guess what question to ask next.

A physician should not repeatedly reconstruct the context behind a clinical decision.

A medical biller should not have to become a detective because essential information is scattered across disconnected systems.

And a practice owner should not have to wait until the end of the month to discover a recurring problem that could have been visible much earlier.

Healthcare does not need technology for technology's sake.

It needs systems that help people do the right work with the right information at the right time.

We have spent years teaching technology to process more work.

Perhaps the next breakthrough will come from designing systems that recognize which problems should never have reached the next step in the first place.

And if that sounds less exciting than another AI announcement, consider this:

Sometimes, the best result is a claim that never needed correcting, an authorization that did not stall, or a patient who did not have to make five phone calls to discover what happens next.

No dramatic alert. No heroic spreadsheet. No billing department operating like a crime-scene investigation unit.

Just a process that works better.

That may not be flashy. But for physicians, staff, and patients, it could be far more valuable.


Frequently asked questions

What is upstream billing intelligence?

It is an approach to identifying and addressing information gaps, requirements, and operational risks before they contribute to claim errors, denials, or rework.

Why do billing problems begin before a claim is submitted?

Claims depend on information collected across registration, eligibility, referrals, authorization, documentation, coding, and charge capture. Errors or omissions at earlier stages can affect the claim later.

Can AI prevent medical billing denials?

AI may help identify patterns, missing information, and potential inconsistencies. It cannot guarantee payment or eliminate every denial. Results depend on data quality, payer rules, workflow integration, and appropriate human oversight.

What should a small practice do first?

Choose one recurring problem, identify where it originates, map the information and handoffs involved, test one targeted improvement, and measure whether the change reduces errors or rework.

Is OnnX 2.0 a traditional medical billing service?

OnnX 2.0 is being developed as an upstream intelligence platform focused on helping physician-owned practices improve the information and decisions that affect billing. Its intended positioning emphasizes prevention and intelligence rather than outsourced billing services.


Join the conversation

Katherine Screws's story raises a question that reaches far beyond transplant medicine:

Are we building smarter healthcare systems—or simply getting better at managing the problems our systems keep creating?

Physicians, practice owners, administrators, and medical billers: Where does the most avoidable rework begin in your experience—registration, eligibility, authorization, documentation, coding, or the handoffs between them?

Share your perspective in the comments. If this challenges how we think about healthcare administration, share or repost it so others can join the discussion.


About the author

Daniel Cham, MD is a physician, entrepreneur, and healthcare technology founder developing OnnX 2.0, an upstream intelligence platform for healthcare built by physicians and medical billers since 1995. His work focuses on improving the quality and continuity of information across clinical and administrative processes so physician-owned practices can reduce preventable billing problems and focus more attention on patient care.


Disclaimer: This article is for educational and informational purposes only and does not provide medical, legal, coding, billing, or reimbursement advice. Katherine Screws's experience is discussed based on public reporting and should not be interpreted as an allegation of wrongdoing by any individual or organization. The comparison with medical billing concerns information and coordination, not equivalence between clinical outcomes and administrative delays.


References

  1. Associated Press, October 20, 2026: Arizona woman's three-year wait for an intestine shows the US organ transplant system's complexity.
  2. Associated Press, October 20, 2026: How the US organ transplant system works and what to ask to improve your chances.
  3. American Medical Association: Survey: Prior authorization reform pledge falls short for physicians.
  4. American Medical Association, September 30, 2026: Statement from leading physician organizations on the role of augmented intelligence in healthcare.
  5. Agency for Healthcare Research and Quality: Care Coordination.

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#Healthcare #PhysicianOwnedPractices #MedicalBilling #HealthcareAdministration #RevenueCycleManagement #PriorAuthorization #ClaimDenials #HealthcareAI #HealthTech #OnnX2.0 #UpstreamIntelligence #PhysicianBurnout

 

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Katherine Screws Waited Three Years for a Transplant. What If Healthcare Is Solving the Wrong Problem?

A patient’s search for answers reveals an uncomfortable truth about complex systems: when information is fragmented, people can follow the p...