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Stereotactic Brain Biopsy Step by Step: Planning Scans, Coordinates and the Needle Path

24 min read
Stereotactic Brain Biopsy Step by Step: Planning Scans, Coordinates and the Needle Path

Key Takeaways

  • Stereotactic means locating a point in the brain with a three-axis coordinate grid, and the biopsy needle simply follows a path planned on the scan.
  • Surgeons usually target the enhancing rim of a lesion rather than its center, because the center is often dead tissue that gives the pathologist nothing to work with.
  • Frame-based, frameless and robotic systems differ in how the plan is transferred to the patient, not in what the tissue can reveal.
  • Brain tissue has no pain receptors, so what is felt during and after the procedure comes from the scalp, skull covering and any frame pin sites.
  • A frozen section gives a provisional answer within minutes, but the final report with stains and molecular tests can take days to a couple of weeks, according to the NHS.
  • Bleeding along the needle track is the risk surgeons plan hardest to avoid, which is why many units perform a CT scan in the hours after the biopsy.
Quick Answer

A stereotactic brain biopsy uses a detailed MRI or CT scan, a three-dimensional coordinate system and a thin needle to remove a tiny sample of brain tissue through an opening in the skull about the width of a pencil. The surgeon plans a target point and a safe path on the scan, matches that plan to the patient's head in the operating room, then guides the needle to the target so a pathologist can examine the tissue.

The consultation room is quiet except for the click of a mouse. On the screen, a grey image of a brain rotates slowly, and somewhere near the middle sits a bright smudge no bigger than a grape. The surgeon says the sentence most people remember afterwards: the scan cannot tell us what this is, so we need a small piece of it. Then comes the question almost everyone asks next, in one form or another: how is a stereotactic brain biopsy done, and how does anyone reach something that deep without harming what surrounds it?

The honest answer is less dramatic than the imagination supplies. There is no large opening, no lifting of the skull. There is a scan, a set of coordinates, a carefully chosen line through the brain, and a needle thinner than a drinking straw that follows that line to a point measured in millimeters.

This explainer walks through each of those steps in order, from the planning scan to the pathology report, and is honest about what the procedure can and cannot tell you.

How is a stereotactic brain biopsy done, in plain language?

Strip away the vocabulary and the procedure has a simple shape. A biopsy is the removal of a small piece of tissue so a pathologist, a doctor who diagnoses disease by studying cells under a microscope, can identify what it is. Stereotactic means locating a point inside the body using a three-dimensional coordinate grid, in much the same way a map reference pins a spot on a mountainside.

Put the two together and you have a way of sampling tissue deep inside the head through an opening the width of a pencil. The steps run in a fixed order. First, a high-resolution MRI or CT scan captures the brain and the abnormal area. Second, the surgical team marks a target point on that scan and chooses an entry point on the scalp, then draws the straight line between them. Third, in the operating room, the scan is matched to the real position of the patient’s head, a step called registration. Fourth, the surgeon makes a small incision and drills a small hole in the skull, known as a burr hole. Fifth, a thin biopsy needle is advanced along the planned line to the planned depth, and several tissue samples, each roughly the size of a grain of rice, are withdrawn. Finally, the needle comes out, the incision is closed, and the tissue goes to the laboratory.

Johns Hopkins Medicine describes this as the least invasive way to obtain brain tissue, and the whole sampling phase is measured in hours rather than a full day. The scan and the coordinates carry most of the work; the needle simply follows the plan. That is the idea worth holding onto as the detail builds in the sections that follow.

Who is usually offered a stereotactic biopsy, and who is asked to wait?

Not every brain abnormality needs a biopsy, and not every biopsy needs a needle. The Mayo Clinic explains that a biopsy is chosen when imaging alone cannot settle what an abnormal area is, and that the tissue may be taken either as a separate needle procedure or as part of a larger operation to remove the lesion.

A stereotactic needle biopsy tends to be the preferred route in a few recognizable situations. The abnormal area may sit deep in the brain, near structures that control movement, language or consciousness, where an open operation would carry more risk than the information justifies. There may be several lesions scattered through the brain, where removing one would not remove the problem. The scan may suggest a condition that is treated without surgery once confirmed, such as lymphoma, an infection or an inflammatory process. Or the person may have other health problems that make a longer operation under general anesthesia unwise.

Others are asked to wait, or are steered toward a different approach. If the surgical team already plans to remove the lesion, the tissue is usually taken during that operation rather than in a separate procedure. If the target is wrapped in large blood vessels, the risk of bleeding along the needle track may outweigh the benefit, and the team may prefer imaging follow-up or a different sampling method. People taking medicines that reduce clotting are typically asked to pause them under the guidance of the prescribing clinician, so timing shifts. Marked brain swelling is often brought under control first. And some scan appearances are characteristic enough that a period of watchful monitoring is reasonable before anyone reaches for a needle. Each of these is a judgment call, made by the treating team with the person in front of them.

What happens at the planning scan for a brain biopsy?

The planning scan is not the same as the scan that found the problem. It is taken specifically for navigation, so it uses thinner image slices, often a millimeter or less, and it is usually done with contrast, a dye injected into a vein that makes abnormal tissue and blood vessels stand out. MedlinePlus notes that a head MRI typically takes 30 to 60 minutes, and a planning study can sit at the longer end because more sequences are collected.

Before the scan, the team needs a way to line up the images with the patient’s head later. There are two broad methods. With a frame-based system, a lightweight rigid frame is fixed to the skull under local anesthetic before scanning, and a set of markers attached to the frame appears on every image. With a frameless system, small adhesive markers called fiducials are stuck to the scalp in a spread pattern, or the team relies on matching the surface contours of the face and forehead. Either way, the markers give the software fixed reference points that exist both in the picture and in the room.

The timing matters. Fiducial stickers can shift if a scalp moves or a pillow rubs against them, so frameless planning scans are usually done the same day or the day before, and the person is asked not to touch the markers. Frame-based scans are almost always done on the day itself with the frame already in place.

What the scan cannot do is tell the surgeon what the lesion is. It shows where the tissue is most abnormal, which part is most likely to be alive rather than dead in the center, and which vessels lie along possible routes. Those three pieces of information drive everything that follows.

From scan to coordinates: how a target becomes three numbers

Once the planning images are loaded, the surgeon works in three dimensions on a screen. The software stacks the thin slices into a digital model of the head, and every point in that model has a coordinate along three axes: left to right, front to back, and top to bottom. Choosing a target means clicking on a point and letting the software report those three values.

Which point? Usually not the middle of the lesion. Many brain abnormalities have a dead or fluid-filled center that gives the pathologist nothing to work with. The surgeon typically aims at the rim or at the area that lights up most strongly with contrast, because that is where living, representative cells are most likely to be found. For lesions that do not enhance, other MRI sequences guide the choice.

Next comes the entry point on the scalp. The software draws a straight line between entry and target and displays the tissue that line passes through on every slice. The surgeon can slide the entry point around the skull and watch the line move, hunting for a route that avoids the structures described in a later section. Some systems also let the team set a second target so several samples can be taken along one track at different depths.

The final step is registration. In the operating room, a pointer or camera touches or sees the fiducials, or the frame’s reference marks, and the software calculates how the scan model sits relative to the actual head. From that moment, the coordinates on the screen correspond to real millimeters in the room. The team checks this by touching a known landmark, such as the tip of the nose, and confirming the cursor lands in the right place on the scan. If it does not, registration is repeated before anything else happens.

Frame-based, frameless and robotic stereotactic biopsy: what changes and what does not

People often hear these three words and assume they describe three different operations. They do not. The scan, the coordinates, the needle and the tissue are the same. What differs is how the head is kept still and how the plan is transferred into the room. Johns Hopkins Medicine describes both frame-based and frameless techniques as standard ways of performing a stereotactic biopsy, and the choice usually reflects the target, the equipment available and the surgeon’s training rather than a difference in what the biopsy can reveal.

Feature Frame-based Frameless (navigation) Robot-assisted
How the head is referenced Rigid frame pinned to the skull under local anesthetic Scalp fiducials or surface matching, head held in a clamp Frame or clamp, plus a robotic arm registered to the scan
When the planning scan is taken Same day, with the frame on Same day or the day before, markers in place Either, depending on the system
How the needle is aimed Mechanical arc set to coordinates Tracked guide aligned by camera Arm positions the guide along the planned line
Typical extra step for the patient Frame pins placed while awake or sedated Care not to disturb stickers Similar to whichever base method is used
What the tissue tells you Same Same Same

Frame-based systems have the longest track record and are mechanically rigid. Frameless systems avoid the pins and allow scanning a day ahead. Robotic arms hold and move the guide with fine control. Published series compare their accuracy in detail, and the differences are generally small relative to the size of most targets. Your team’s choice is a reasonable question to ask, but it is rarely the thing that decides whether the biopsy answers your question.

How surgeons choose the needle path in a brain needle biopsy procedure

If the target is the destination, the trajectory is the road. Choosing it is where much of the surgical judgment lives, and the rules are consistent enough to describe.

The route is kept as short and as straight as the anatomy allows, because every millimeter of brain the needle passes through is a millimeter that could bleed or swell. It avoids blood vessels visible on the contrast scan, particularly the larger ones running on the surface and in the grooves of the brain. It steers clear of the sulci, the folds on the brain’s surface, because vessels live in those folds and because entering through the crown of a fold gives a more predictable path. It avoids the ventricles, the fluid-filled chambers in the center of the brain, since crossing them can cause bleeding into the fluid and can let the needle drift.

The path also avoids what neurosurgeons call eloquent cortex: regions whose injury would produce an obvious loss of function, such as the strips controlling movement and sensation, the language areas of the dominant side, and the visual pathways at the back. When a target sits inside such a region, the surgeon may approach it from a direction that passes through less critical tissue, even if that means a longer track.

Finally, the surgeon thinks about the tissue itself. A track that enters the enhancing rim of a lesion at an angle can allow two or three samples from slightly different depths, which improves the chance that at least one contains diagnostic cells. Where a lesion is heterogeneous, mixed in appearance on the scan, sampling more than one part can matter for grading. All of this is decided before the first incision, on the screen, where changing a plan costs nothing.

How is a stereotactic brain biopsy done on the day, step by step?

The morning usually begins in a preoperative area with the ordinary checks: identity, consent, a review of medicines, and the marking of the side. The anesthesia team then explains the plan for the procedure. Johns Hopkins Medicine notes that a stereotactic biopsy may be done under general anesthesia or under local anesthetic with sedation, so some people sleep throughout and others are drowsy but rousable. The choice depends on the target, the person’s health and the team’s routine.

If a frame is used, it is fixed to the skull with pins after the scalp is numbed at four points. If a frameless system is used, the head is settled into a padded clamp. Registration follows, as described earlier, and the team confirms accuracy before proceeding.

A small patch of hair at the entry point is usually clipped rather than the whole head shaved. The scalp is cleaned and numbed, and an incision roughly the length of a fingertip is made. A burr hole, a small round opening in the skull drilled with a guarded bit, is created; it is about the width of a pencil. The dura, the tough membrane covering the brain, is opened with a tiny cut, and the guide is set to the planned trajectory and depth.

The biopsy needle itself is a thin tube with a side window. It is advanced slowly along the track to the target depth. Gentle suction draws a sliver of tissue into the window, an inner cutting sleeve rotates to separate it, and the needle is withdrawn with the sample inside. This is repeated two to four times, sometimes at more than one depth. A sample may be sent immediately for a rapid look, covered in the next section. The surgeon watches for bleeding from the track, waits if needed, then removes the needle. The dura is left or sealed, the burr hole may be covered with a small cap, and the scalp is closed with sutures or staples.

What happens to the tissue, and how long do brain biopsy results take?

The samples are small, and the laboratory work is where the biopsy earns its purpose. Two processes usually run in parallel.

The first is the frozen section, a quick check performed while the person is still in the operating room. A sample is frozen, sliced thinly and stained within minutes. The pathologist’s goal at this stage is narrow: to confirm that the tissue is abnormal and representative, not to give a final name. If the frozen section shows only normal brain or dead tissue, the surgeon can take another sample from a slightly different depth before closing. This step is one of the main reasons stereotactic biopsies so often return a usable answer.

The second process is the permanent section. The remaining tissue is preserved, embedded in wax, sliced far more finely and stained with a panel of dyes. Immunohistochemistry, the use of antibodies that light up specific proteins, helps distinguish tumor types and tell tumors apart from lymphoma, infection or inflammation. For many brain tumors, molecular tests that look for specific gene changes are now part of the standard report because they affect how the condition is classified and managed. The NHS explains that biopsy results in general can take from a few days to a couple of weeks, and molecular testing can add time beyond that.

It helps to know in advance that there may be two conversations: an early one after the frozen section, which is provisional, and a later one when the full report is complete. The early impression is occasionally revised. Ask your team which of those two conversations you are having when results are discussed, and when the final report is expected.

How painful is a stereotactic biopsy?

This question deserves a straight answer, and the anatomy supplies a reassuring one. Brain tissue itself has no pain receptors. The needle passing through the brain is not felt. What can be felt, and what the anesthetic plan targets, is the scalp, the skull’s outer covering and the membranes around the brain.

Under general anesthesia, nothing is felt during the procedure. Under local anesthetic with sedation, people commonly describe pressure and vibration during the drilling, a sensation many compare to dental work, and the brief sting of the numbing injections at the pin sites or incision. The sedation is adjusted by the anesthesia team throughout, and speaking up about discomfort is expected rather than frowned upon.

Afterwards, the most common complaint is a headache centered on the incision and, if a frame was used, on the pin sites. Johns Hopkins Medicine lists headache among the expected effects after a brain biopsy and describes it as manageable with pain relief prescribed by the care team. Some people notice tenderness when lying on that side of the head for a few nights, and a small area of scalp numbness around the incision is common and usually settles over weeks.

A different kind of headache is the one to take seriously: sudden, severe, unlike the incision ache, or accompanied by drowsiness, vomiting or new weakness. That pattern can signal bleeding and belongs in the red-flag section later in this article, not in a discussion of ordinary soreness.

One more honest point. The anticipation is frequently worse than the experience. People who were dreading the frame or the drill often say afterwards that the waiting for the pathology report was the hardest part. That is not a reason to dismiss the fear, only a reason to know it is common.

What are the main brain biopsy risks, and how often is the result non-diagnostic?

A small opening does not mean a risk-free procedure, and a candid team will say so. Johns Hopkins Medicine lists the principal risks of brain biopsy as bleeding, infection, seizures, brain swelling and stroke or new neurological symptoms, and the Mayo Clinic adds the general risks that come with any anesthesia.

Bleeding is the one surgeons think about most, because it can happen along the needle track or at the target and because the skull leaves little room for a blood clot to expand. Most bleeds are tiny, cause no symptoms and are noticed only on a routine scan after the procedure, which many teams perform for exactly this reason. A minority cause new symptoms, and a small number require further surgery. Risk is higher when the target is very vascular, when the lesion is a type that bleeds easily, or when blood clotting is impaired, which is why medicines that affect clotting are reviewed in advance with the prescribing clinician.

Seizures can occur because the needle irritates the brain’s surface. People who have already had seizures are usually kept on their existing treatment, and the team decides whether short-term preventive medicine is appropriate. Infection at the wound or, rarely, deeper in the brain is uncommon and is reduced by sterile technique and, in many units, a single dose of antibiotic at the time of surgery, chosen by the team.

Then there is the risk that the biopsy does not answer the question. Published surgical series describe most stereotactic biopsies yielding a diagnosis, with a minority returning tissue that is normal, dead or too small to classify; the exact proportion varies with the type of lesion and the sampling technique. A non-diagnostic result is disappointing, not dangerous, and the options are usually another biopsy, an open procedure or continued imaging. Your team can put numbers to these risks for your specific target, and those numbers matter more than any general figure.

How long does it take to recover from a stereotactic brain biopsy? Stereotactic biopsy recovery time explained

Recovery from the needle procedure is usually faster than people expect, though the emotional recovery while waiting for results runs on its own timetable.

The first hours are spent in a recovery area with regular checks of alertness, limb strength and speech. Many units obtain a CT scan of the head during this period to look for bleeding. Johns Hopkins Medicine describes a hospital stay of a night or so as typical after a needle biopsy, with some people going home the same day and others staying longer if there is swelling, a seizure or another reason for caution. The treating team decides, and the decision reflects what happened during the procedure rather than a fixed rule.

At home, the incision is kept clean and dry as instructed. Sutures or staples are typically removed at a follow-up visit within a couple of weeks. Headache and scalp soreness ease over several days. Fatigue is common and tends to lift within a week or two. Light activity, walking and desk-type work are often resumed within days, while heavier exertion, contact sports and anything that risks a blow to the head are usually held back until the wound has healed and the team has reviewed the scan.

Driving is a separate question. Anyone who has had a seizure, or whose lesion raises the risk of one, will be given specific guidance that may extend well beyond the wound-healing period, and it is worth asking about this before discharge rather than assuming.

The pathology report, as described earlier, arrives in days to a couple of weeks, and the follow-up appointment to discuss it is often the true end of the biopsy episode. What comes next depends on that report, and the team will lay out the options, including watchful waiting, at that visit.

What people often get wrong about stereotactic brain biopsy

Because the procedure is unfamiliar and the stakes feel high, a set of misunderstandings comes up again and again. Correcting them is part of preparing well.

The first is that a needle biopsy means the problem is inoperable. It does not. Needle biopsy is chosen when tissue is needed before deciding on treatment, when the lesion is one that is not treated by removal, or when several lesions are present. Plenty of people go on to have a larger operation after a biopsy, and plenty never need one.

The second is that pushing a needle through a tumor spreads it. Tumor cells tracking along a biopsy path is a recognized concern for some cancers elsewhere in the body, but for brain biopsies it is considered very uncommon and does not alter how the procedure is planned or advised.

The third is that the result comes back the same day. The frozen section gives a quick, provisional impression. The final report, including the stains and molecular tests that increasingly define brain tumors, takes longer, and the two can differ.

The fourth is that a biopsy always gives an answer. Most do, but a minority return tissue that cannot be classified, and a second procedure is sometimes needed. Knowing this in advance softens the disappointment if it happens.

The fifth is that the robot or the navigation system does the surgery. These tools hold the guide and transfer the plan into the room. A surgeon chooses the target, plans the path, controls the needle and decides when enough tissue has been taken.

The last is that a small incision means negligible risk. Bleeding, seizure and infection are uncommon but real, which is exactly why the planning described in this article is so deliberate. A frank conversation about your own risk is worth more than reassurance from a general figure.

Questions to ask your care team before a stereotactic brain biopsy

A biopsy consultation moves quickly, and the questions that matter most tend to surface on the drive home. Writing a few down beforehand changes the conversation. The list below is a starting point; choose the ones that fit your situation.

  • Why is a needle biopsy being recommended rather than removing the lesion, or rather than waiting and rescanning?
  • What are the likeliest diagnoses on the current scan, and how would each change the plan?
  • Which part of the lesion will be targeted, and why that part?
  • Will a frame or a frameless system be used, and what will I feel at each stage?
  • Will I be asleep, or awake with sedation, and who decides?
  • What are the specific risks for my target, particularly of bleeding, given where it sits?
  • How likely is it that the sample will not give a diagnosis, and what would happen then?
  • Which of my regular medicines need to be paused or continued, and who will give me those instructions?
  • Will I have a scan after the procedure, and what is it looking for?
  • How long is the expected hospital stay, and what would make it longer?
  • When will I hear the provisional result, and when the final report?
  • Who do I contact, day or night, if something feels wrong after I go home?
  • What are the rules about driving, work, exercise and travel while I wait for results?

Bring someone with you if you can. Two sets of ears catch more, and the person facing the biopsy is often the one least able to take notes. Ask for a written summary or a copy of the letter, and ask which member of the team is the right first call for questions that arise later. The decision to proceed, to wait or to choose another route always rests with you and your treating team together.

When to call your doctor after a stereotactic brain biopsy

Most people leave hospital with a sore scalp, a mild headache and a follow-up date, and that is the whole story. A small number develop a problem in the first days, and the difference between a good outcome and a difficult one often comes down to how quickly it is recognized. Johns Hopkins Medicine advises contacting the care team promptly for the warning signs below, and the guidance holds for any brain procedure.

Call emergency services, or have someone call for you, if any of the following appear suddenly: a severe headache that is different from the incision ache and does not ease; new weakness, numbness or clumsiness in the face, an arm or a leg; slurred speech, trouble finding words or difficulty understanding others; sudden confusion, unusual drowsiness or difficulty staying awake; a seizure, whether or not you have had one before; repeated vomiting; or a sudden change in vision. These can indicate bleeding or swelling at the biopsy site, and time matters.

Contact the care team the same day, without waiting for the scheduled visit, if you notice a fever or chills; redness, warmth, swelling or discharge at the incision; the wound edges separating or clear fluid leaking from it; a stiff neck with headache and sensitivity to light; a headache that is steadily worsening over a day or two rather than easing; or new symptoms that resemble those that led to the scan in the first place.

If you are unsure whether something counts, treat it as though it does. Teams would far rather field a call about a headache that turns out to be ordinary than learn about one that was not. Keep the emergency contact details you were given somewhere visible, and make sure whoever is with you at home knows where they are and what to look for.

Frequently asked questions

How long does it take to recover from a stereotactic brain biopsy?

Most people are home within a day or so and back to light activity within days, with the incision healing over about two weeks. Johns Hopkins Medicine describes a brief hospital stay as typical after a needle biopsy. Fatigue and scalp soreness ease over the first week or two. Heavier exertion and driving depend on individual advice from the treating team, especially if there has been a seizure.

How painful is a stereotactic biopsy?

The procedure itself is not felt as pain inside the brain, because brain tissue lacks pain receptors. Under general anesthesia nothing is felt; under sedation with local anesthetic, people describe pressure and vibration during drilling and a sting from numbing injections. Afterwards, a headache around the incision and any pin sites is common and is managed with pain relief chosen by the care team.

How often are stereotactic biopsies cancerous?

There is no single honest figure, because the answer depends entirely on why the biopsy was ordered. Biopsies are done for suspected tumors, but also for suspected lymphoma, infection, inflammation and demyelinating conditions, and some tumors found are benign or slow-growing. The Mayo Clinic notes that the scan alone often cannot distinguish these, which is the reason tissue is taken in the first place.

What is stereotactic biopsy recovery time for returning to work?

Desk-based work is often possible within a week or two once headache and fatigue settle, while physically demanding jobs usually wait until the wound has healed and the post-procedure scan has been reviewed. Anyone whose role involves driving or operating machinery needs specific clearance, because seizure risk after a brain procedure can carry restrictions that last longer than wound healing. Your team sets the timeline.

What is a frameless stereotactic brain biopsy?

A frameless stereotactic brain biopsy uses adhesive scalp markers or facial surface matching, tracked by a camera, to align the planning scan with the head instead of a rigid frame pinned to the skull. The head is held in a padded clamp, and the needle guide is aimed along the planned path using the navigation display. The target, needle and tissue analysis are the same as in frame-based biopsy.

What are the main brain biopsy risks I should know about?

Johns Hopkins Medicine lists bleeding, infection, seizures, brain swelling and new neurological symptoms as the principal risks, alongside general anesthetic risks noted by the Mayo Clinic. Bleeding along the needle track is the one surgeons plan most carefully to avoid. There is also the possibility that the sample does not yield a diagnosis and a further procedure is needed. Ask your team for risk estimates specific to your target.

Will I be awake during the brain needle biopsy procedure?

It depends on the team’s plan and your health. Stereotactic biopsies are performed either under general anesthesia, where you are fully asleep, or under local anesthetic with sedation, where you are drowsy but can respond. Frame placement, when used, is done after the pin sites are numbed. The anesthesia team will explain which approach is proposed and why, and you can raise preferences before the day.

Can a stereotactic biopsy miss the diagnosis?

Yes, in a minority of cases the tissue turns out to be normal, dead or too scant to classify, a result called non-diagnostic. Sampling the enhancing rim rather than the center, taking several samples and checking a frozen section during the procedure all reduce this chance. When it happens, options include a repeat biopsy, an open procedure or continued imaging, decided with the treating team.

How long until brain biopsy results come back?

A provisional impression from the frozen section is often available during or immediately after the procedure. The full report, including special stains and molecular tests, takes longer; the NHS describes biopsy results in general as taking from a few days to a couple of weeks, and molecular work can extend that. Ask which result you are being given, as the provisional view is occasionally revised.

Will my head be shaved for a stereotactic biopsy?

Usually not. Most teams clip only a small patch of hair around the planned entry point, roughly the size of a coin, so the surrounding hair can cover the incision as it heals. Frame pin sites, when a frame is used, generally do not require clipping. If your scalp markers must stay in place overnight, you will be asked not to wash or brush over them.

References

This article is for general information only and is not a substitute for professional medical advice. Please consult a qualified doctor about your individual situation.

Dr. Şule Eren
Dr. Şule Eren, MD
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Published October 10, 2026
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