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Pulmonary Fibrosis: 3D Lung Simulation of Airflow & Inhaled Air Volume

🫁 Senior High School (grades 9–12) · restrictive lung disease · spirometry
A student in the Philippines asked: how does air flow into scarred lungs, and how much less air can they take in? Breathe in with healthy lungs and lungs with pulmonary fibrosis side by side, drag the severity slider, then measure the difference with a spirometry lab, zoom into the alveolus, compare lung compliance and try a walk test.
New to breathing? Start with The Respiratory System (3D) and Gas Exchange. This page is for learning, not medical advice.

🫁 Lung Lab: healthy lungs and pulmonary fibrosis, side by side

What you will do: breathe in with both lungs, make the scarring worse with the slider and see how the air you can take in shrinks. In pulmonary fibrosis the lung tissue is scarred and stiff, so the lungs cannot stretch. Done in about 30 minutes: finish the 7-step mission below.

  1. 1 Predict & max breath
  2. 2 Spirometry: 3 runs
  3. 3 Alveolus
  4. 4 Compliance
  5. 5 Walk test
  6. 6 Label lab
  7. 7 Quiz 7/10

Mission progress: 0 / 7

Lung LabAirflow and the air you can breathe in
Illustration, not a patient scan · typical adult values
Answer the prediction first →

3D model: Z-Anatomy (CC BY-SA 4.0), based on BodyParts3D © The Database Center for Life Science (CC BY-SA 2.1 Japan); bronchial tree from the Human Reference Atlas (HuBMAP, NIH; CC BY 4.0). Simplified by SciSim. The scarring, color change and shrinking of the fibrotic lungs are made in your browser to show the idea: this is an illustration, not a patient scan.

How to use this lab
  • Severity slider (or the presets): 0 = healthy lungs, 100 = very severe fibrosis. The right-hand lungs change, the left ones stay healthy.
  • Breathe / Pause: calm breathing. Watch the blue (in) and amber (out) air dots and the number of liters. The fibrosis lungs breathe faster but take in less each time.
  • Max breath: the deepest breath in, then a hard breath out. This is what spirometry measures (answer the prediction first).
  • Drag the lungs to turn them, scroll or pinch to zoom. Keyboard: click the lungs, then use the arrow keys and + / −.

📈 Spirometry lab: how much air, and how fast?

Task: run the test for a healthy person, for pulmonary fibrosis (restrictive) and for asthma/COPD (obstructive) and press Record each time. Done when the table holds all three kinds. In spirometry you breathe in as far as you can, then blow out as hard and as long as you can into a tube. The machine records the volume of air.

Who is breathing into the tube?

Answer the prediction first.

My data table

#LungsSeverityTLC (L)FVC (L)FEV₁ (L)FEV₁/FVCFVC, % of normalPattern

No runs yet. Press Run the test, then Record this run.

Read the graph: the plateau is the biggest volume. In restriction (fibrosis) the volumes are small, but the air still leaves fast, so FEV₁/FVC is normal or high (about 0.80–0.90). In obstruction (asthma/COPD) the air leaves slowly, FEV₁/FVC is below about 0.70, and the lungs trap air (residual volume goes up). Shapes are simplified; values are typical, not a diagnosis. In real patients the ratio is often 0.80–0.90 and does not rise smoothly with severity: the slider draws a small rise only to show the idea (stiff lungs recoil strongly, so the small amount of air leaves fast).

🔬 Zoom in: the alveolus and the scarred wall

Task: watch oxygen cross the wall between the air and the blood. Predict, then let the scar tissue build up. Done when you have run the animation once and set the exercise slider to hard exercise. The picture is a simplified drawing; the wall is drawn much thicker than real (0.5 µm is far too thin to see).

oxygen (O₂)collagen scar fibersred blood cell

Answer the prediction first.

Wall thickness0.5 µm (normal)
Gas transfer (relative)100% of normal
Blood passes in0.75 s
Blood oxygen saturation, healthy97%
Blood oxygen saturation, fibrosis97%

Fick’s law (the idea): the rate of diffusion is about (area × pressure difference) ÷ wall thickness. A thicker wall and fewer working air sacs mean slower oxygen transfer. At rest the blood spends about 0.75 s in the capillary and there is time; in hard exercise it passes in about 0.25 s, so a scarred lung runs out of time. Saturation values come from a simple illustrative model (not a patient measurement).

🎈 Compliance: how much pressure does a liter of air need?

Task: inflate both lungs with the pressure slider and compare. Done when you have measured how much pressure +1 liter needs for healthy lungs and for fibrosis (set the severity above 0). Compliance C = ΔV ÷ ΔP tells how easily a lung stretches: a thin balloon has high compliance, a stiff rubber ball low compliance.

healthypulmonary fibrosis

Answer the prediction first.

HealthyFibrosis
Volume at this pressure2.3 L2.3 L
Added above resting volume0.0 L0.0 L
Pressure for +1 L4.1 cmH₂O4.1 cmH₂O
Compliance C0.200.20

C in liters per cmH₂O, measured near normal breathing.

Why it matters: stiff lungs need much more effort (a bigger pressure change by the breathing muscles) for the same breath, so the person breathes in small, quick breaths. Healthy C ≈ 0.20 L/cmH₂O in this model; at severity 50 it is about 0.11 and at severity 80 about 0.07. Real values vary between people and the curve is simplified.

🚶 Walk test: oxygen and effort

Task: doctors use a six-minute walk test. In this simplified version six minutes pass in about 30 seconds. Done when both walkers have finished one test at a brisk pace with a severity above 0. The numbers are illustrative, not real patient data.

healthypulmonary fibrosis88% warning line

Answer the prediction first.

HealthyFibrosis
Time0:00 of 6:00
Distance0 m0 m
Breaths per minute1212
Blood oxygen (SpO₂)97%97%
Lowest SpO₂––

Remember: in clinics a fall to 88% or below on exertion is a recognized warning sign (it is often used when deciding about oxygen treatment). People with fibrosis may have a normal oxygen level at rest and drop only when they move. A pulse oximeter on a finger measures SpO₂. This is a teaching model, not a medical test.

💡 The Idea, Step by Step

1. Everyday picture: a stretchy balloon and a stiff one

Blow into a new balloon: the first puff is hard, then it stretches and gets easy. Now try a thick, stiff rubber ball with the same effort: hardly any air goes in. Healthy lungs are like the stretchy balloon, with thin walls that give way easily. In pulmonary fibrosis (fibro- = scar tissue) scar tissue builds up in the lung around the tiny air sacs. The lung becomes thick and stiff, like the ball, so less air goes in with each breath, and the scars do not go away.

2. Name the volumes

A calm breath moves the tidal volume (about 0.5 L in a healthy adult). The biggest breath you can blow out after the deepest breath in is the vital capacity; when it is blown out hard it is called the forced vital capacity (FVC), about 4.6 L. Some air always stays in the lungs, the residual volume (RV), about 1.2 L. Together they make the total lung capacity (TLC) ≈ 5.8 L. FEV₁ is the volume blown out in the first second (about 3.7 L), and the ratio FEV₁/FVC (about 0.80) tells how fast the air leaves.

These are approximate values for a healthy adult; they change with sex, age and height. In this simulator, moderate fibrosis (severity 50) gives FVC ≈ 2.8 L (60% of normal) and TLC ≈ 3.9 L. In one maximal breath the lungs take in 2.1 L instead of 3.5 L.

3. Why? Stiffness, a thick wall, and open airways

Stiff lungs. Compliance C = ΔV ÷ ΔP falls from about 0.20 to about 0.11 L per cmH₂O. Each liter needs more pressure, so each breath is smaller (0.42 L instead of 0.50 L) and the breathing rate rises (20 instead of 12 per minute). Thick wall. The wall between air and blood grows from about 0.5 µm to about 1.5 µm, and by Fick’s law the diffusion rate is about (area × pressure difference) ÷ thickness, so oxygen crosses more slowly. In exercise blood rushes past quicker, and the oxygen level in the blood can fall. Open airways. The tubes are not blocked, so the small amount of air leaves quickly: FEV₁/FVC stays normal or even rises (0.85). This is the key difference from asthma and COPD, where narrowed airways slow the air down and FEV₁/FVC falls below about 0.70.

4. Try this in the simulator

  • Lung Lab: press Moderate, then Max breath. Compare the liters inhaled by the two sets of lungs and the diaphragm and rib movement.
  • Spirometry lab: record Healthy, Pulmonary fibrosis and Asthma/COPD at severity 50. Which one has a low FEV₁/FVC? Which one has a small TLC?
  • Walk test: set the severity to 80 and walk at a brisk pace. Does the oxygen fall below the 88% warning line?
Deeper (AP / first-year college): formulas and worked examples
  • Static compliance C = ΔV ÷ ΔP. Healthy lungs: 0.5 L for 2.5 cmH₂O gives 0.20 L/cmH₂O. A stiff lung with C = 0.10 L/cmH₂O needs 5 cmH₂O for the same 0.5 L. Compliance is the inverse of elastance (stiffness), E = 1/C. In the model the lung curve is a smooth S-shape and C is measured near the resting volume.
  • FEV₁/FVC. Healthy: 3.68 ÷ 4.60 = 0.80. Pulmonary fibrosis (severity 50): 2.35 ÷ 2.76 = 0.85. Asthma/COPD example (severity 50): 2.15 ÷ 3.91 = 0.55. A ratio below about 0.70 (or below the lower limit of normal for that person) means obstruction.
  • Percent of predicted = measured ÷ predicted × 100. Predicted values come from reference equations (sex, age, height, ancestry), so a healthy person can differ from the textbook value. FVC at 2.76 L is 60% of 4.6 L (2.8 L rounded). Fibrosis is often graded by FVC % predicted: mild about 70–80%, moderate 50–69%, severe below 50% (together with the gas-transfer test DLCO).
  • Restriction is defined by a low TLC (below the lower limit of normal, often about 80% of predicted). It can have causes outside the lung tissue, for example a stiff chest wall, weak muscles, obesity or fluid or air around the lung, so doctors look at the whole picture.
  • Fick’s law for a thin membrane: rate ∝ (area × pressure difference) ÷ thickness. If thickness triples and the other factors stay the same, the rate falls to one third. DLCO (diffusing capacity for carbon monoxide) is the clinical test of gas transfer; it falls in fibrosis because of the thick wall and lost capillaries.

🧬 Causes, signs and care (overview)

What it is

Pulmonary fibrosis (PF) is scarring of the lung tissue: too much collagen builds up in the interstitium, the thin tissue around the alveoli. The walls get thick and stiff, and the scarring is irreversible. Idiopathic pulmonary fibrosis (IPF) is the common form with no known cause; it mostly affects older adults.

Known causes and risk factors

  • Breathing in dusts over many years: asbestos, silica, coal and some other dusts
  • Some medicines (for example bleomycin, amiodarone, nitrofurantoin)
  • Radiation treatment to the chest
  • Connective-tissue (autoimmune) diseases such as rheumatoid arthritis or scleroderma
  • Hypersensitivity pneumonitis (an allergic reaction to inhaled dusts or molds)
  • For IPF: older age, a history of cigarette smoking, stomach-acid reflux (GERD) and genes are associated factors; the cause is still not known

Signs and symptoms

A dry, long-lasting cough and shortness of breath, first with effort, then even at rest; fast, shallow breathing; tiredness; in some people, rounded, widened fingertips (clubbing). Crackling sounds in the lungs can be heard with a stethoscope.

How it is found

A doctor listens to the chest and asks about work, medicines and family; then spirometry (FVC, FEV₁), a gas-transfer test (DLCO), an oxygen level (pulse oximeter, walk test) and a high-resolution CT scan of the chest.

Care

Antifibrotic medicines (pirfenidone, nintedanib) can slow the loss of lung function; they do not reverse the scarring. Other parts of care: oxygen therapy when needed, pulmonary rehabilitation (exercise and breathing training), vaccinations, treating the cause if one is found, and lung transplant for some selected patients.

Educational, not medical advice. This page is a simplified model for learning. Anyone with a long-lasting cough or breathlessness should talk to a doctor or nurse.

🏷️ Label Lab: the Breathing Tract, Label Quiz & Jobs

Pulmonary fibrosis scars the tissue around the alveoli, the air sacs at the very end of the airways. Know where they are first. Pick Basic (6 labels) or Advanced (10). Switch between the labeled diagram, a blank one, a label quiz and match the jobs. Score 70% or more in the label quiz to finish mission step 6. On a phone, swipe the diagram sideways.

Level:
Simplified, not a patient scan · scisim.org

    Tap a word, then tap the numbered box it belongs to (on the diagram or in the list below). Tap a filled box to take the word back.

    Each line describes the job of one part. Tap a part name, then tap the box next to the job it does. Tap a filled box to take the word back.

    Download:

    ✅ Quiz: 20 questions, 10 per round

    Pick Round 1 or Round 2. Each round has 10 questions (at least 4 on reading spirometry values and graphs). Answer, read the explanation, go on. 7 or more right completes the mission.

    📝 Printable worksheet and answer key

    A two-part print-out: the student worksheet (it includes the rows from your spirometry table if you recorded some) and a separate answer key page for the teacher. Opens in a new window: press Print or save as PDF.

    Numbers in the worksheet and its key come from the same model as the simulator (typical adult, severity presets 0, 25, 50 and 80).

    👩‍🏫 For teachers

    A 45-minute lesson for Senior High School biology (grades 9–12; includes data-interpretation skills): how structure (scarred, stiff tissue) changes function (airflow, air volume, gas exchange). The page works on phones, Chromebooks (1366×768) and without WebGL. Students make a result code (under the simulator) that shows time on task, mission steps and quiz score; you can read it at scisim.org/check. Nothing is sent to a server.

    45-minute plan (each step jumps to a section)

    TimeStepWhat students doGo to
    0–5 minHook and predictShow the Lung Lab on the board. Students answer the prediction, then press Max breath.Lung Lab
    5–15 minExplorePairs try Mild, Moderate and Severe. They write down air inhaled in a max breath (healthy vs fibrosis) and describe how the lungs look and move.Lung Lab
    15–27 minSpirometry labRecord a healthy, a fibrosis and an asthma/COPD run. Students fill the data table and work out which pattern is restrictive and which is obstructive.Spirometry
    27–35 minWhy? Alveolus and complianceThe thick wall slows oxygen (Fick); stiff lungs need more pressure. Do one of the two labs, or split the class.Alveolus / Compliance
    35–42 minWalk test or label labWalk test: does oxygen fall below 88%? Or label the airway diagram.Walk test / Label lab
    42–45 minExit ticket and result codeExit ticket: students write two sentences (why is FEV₁/FVC not low in pulmonary fibrosis?), make their result code and submit it with a photo or PDF of the data table. The 10-question quiz round fits as homework or extra time.Quiz

    Discussion questions

    1. Why can a person with pulmonary fibrosis have a normal FEV₁/FVC but a low FVC? Explain with “airways” and “stiffness”.
    2. Why do people with fibrosis breathe fast and shallow? Link your answer to compliance and the work of breathing.
    3. A scarred wall is 3 times thicker. By Fick’s law, what happens to the diffusion rate? What other factors matter in a real lung?
    4. Why can oxygen be normal at rest but fall during exercise?
    5. Compare asthma and pulmonary fibrosis: which part of the lung is affected, what happens to FEV₁/FVC and TLC, and what could help each?
    6. Which workplaces or hobbies could expose people to dust that harms the lungs, and how could dust exposure be reduced?
    7. Antifibrotic drugs slow the disease but cannot remove scars. Why is early diagnosis important?
    8. The model uses “typical adult” values. How would the numbers change for a tall person, a child or an older person, and why does a doctor use “% of predicted”?

    Vocabulary

    • Alveolus (plural alveoli): tiny air sac where oxygen enters the blood
    • Interstitium: thin tissue around the alveoli and capillaries, where scarring forms
    • Fibrosis: scarring; too much collagen replaces normal tissue
    • Restrictive: lungs cannot expand fully (small volumes, FEV₁/FVC normal or high)
    • Obstructive: airways narrowed, air leaves slowly (FEV₁/FVC low)
    • Spirometry: test that measures how much air and how fast
    • FVC: forced vital capacity: most air blown out after the deepest breath in
    • FEV₁: volume blown out in the first second
    • TLC: total lung capacity: air in the lungs after the deepest breath in
    • Residual volume: air that stays in the lungs after a full breath out
    • Tidal volume: air moved in a calm breath
    • Compliance: C = ΔV/ΔP: how easily the lungs stretch
    • SpO₂: blood oxygen saturation measured by a pulse oximeter
    • DLCO: test of how well gases cross the lung wall

    Common misconceptions

    See the six misconceptions below; each is answered on the page.

    What to ask students to submit

    • The result code (name + code).
    • A photo or PDF of the data table from the Spirometry lab (Print button) or the printed worksheet.
    • Two sentences: Why is FEV₁/FVC not low in pulmonary fibrosis?

    Answer keys

    Expected values in the simulator (typical adult; severity presets)
    Sev.GradeFVC (L)TLC (L), % of 5.8FEV₁ (L), % of 3.68FEV₁/FVCCalm breath (L)Breaths/minC (L/cmH₂O)SpO₂ rest / brisk walk6-min walk (m)
    0normal range4.65.8 (100%)3.68 (100%)0.800.50120.2097% / 96%564 m
    25mild3.64.7 (82%)2.96 (80%)0.830.46160.1597% / 95%501 m
    50moderate2.83.9 (67%)2.35 (64%)0.850.42200.1196% / 92%437 m
    80severe2.03.1 (53%)1.77 (48%)0.880.38250.0795% / 86%361 m
    100severe1.72.7 (46%)1.49 (40%)0.900.35280.0694% / 79%310 m

    Healthy reference: TV 0.5, IRV 3.0, ERV 1.1, RV 1.2 L (IC 3.5, VC 4.6, FRC 2.3, TLC 5.8 L), FEV₁/FVC 0.80, 12 breaths/min, C 0.20 L/cmH₂O. Restrictive: FVC % predicted = 100 − 0.96 s + 0.0032 s²; RV = 1.2 (1 − 0.0015 s); FEV₁/FVC = 0.80 + 0.001 s. The obstructive example uses the same slider: FEV₁/FVC = 0.80 − 0.005 s, RV rises (air trapping). Walk-test and oxygen values are illustrative.

    Quiz answer key (20 questions)
    #QuestionCorrect answer
    1What is pulmonary fibrosis?Scarring (extra collagen) in the lung tissue around the air sacs, which makes the lungs thick and stiff
    2Where does the scarring of pulmonary fibrosis build up?In the thin tissue between the air sacs (alveoli) and the blood capillaries
    3Why does a thicker alveolar wall make it harder to get oxygen into the blood?Oxygen has a longer way to diffuse, and the rate of diffusion is proportional to 1 / thickness (Fick’s law)
    4A patient’s FVC is 2.3 L (predicted 4.6 L) and FEV₁/FVC is 0.86. Which pattern fits?Restrictive, as in pulmonary fibrosis
    5A person blows out 3.0 L in total (FVC) and 1.5 L of it in the first second (FEV₁). What is FEV₁/FVC and what does it suggest?0.50: obstruction (slow emptying)
    6Which breathing pattern is typical for a person with moderate pulmonary fibrosis at rest?Fast and shallow
    7On a volume–time graph of a forced breath, how does the curve of a person with pulmonary fibrosis compare with a healthy person’s?It levels off at a lower volume (smaller FVC) but still rises steeply
    8What can antifibrotic medicines such as pirfenidone and nintedanib do?Slow down the loss of lung function; they do not remove scars that already formed
    9A person’s FEV₁ is 2.4 L and the predicted value for them is 3.7 L. What is FEV₁ as a percentage of predicted?About 65%
    10Lung compliance is C = ΔV / ΔP. A stiff, fibrotic lung has…low compliance: a big pressure change gives only a small volume change
    11Which result shows a RESTRICTIVE pattern best?Low total lung capacity and low FVC, with a normal or high FEV₁/FVC
    12The healthy FVC is 4.6 L. A patient with fibrosis has an FVC of 2.8 L. About what percent of normal is that?About 61%
    13Why is FEV₁/FVC NOT low in pulmonary fibrosis?The airways are open, so air leaves quickly; FEV₁ and FVC both fall together and their ratio stays normal or rises
    14A forced-breath curve levels off at 3.0 L, and 2.55 L has been blown out after 1 second. What is FEV₁/FVC?0.85
    15On a pressure–volume graph, the curve of fibrotic lungs compared with healthy lungs is…flatter and lower: more pressure is needed for the same volume
    16Which of these is a known cause or risk factor for pulmonary fibrosis?Breathing in asbestos or silica dust over many years
    17If an alveolar wall becomes 3 times thicker and nothing else changes, the diffusion of oxygen through it becomes about…one third as fast
    18Which of these lung diseases is OBSTRUCTIVE rather than restrictive?Asthma
    19During a walking test the blood oxygen saturation (SpO₂) of a patient falls from 95% to 86%. What does this tell us?Oxygen drops with effort: a warning sign (88% or lower is often used as a limit) when doctors decide about oxygen treatment
    20Which is a general part of care for people with pulmonary fibrosis (not a cure)?Pulmonary rehabilitation, vaccinations and, when needed, oxygen therapy

    The worksheet answer key is on the second page of the worksheet (open it in the worksheet section).

    ⚠️ Six common misconceptions

    Wrong idea “Pulmonary fibrosis blocks the airways, like asthma.”
    Right idea No. The airways are open. The tissue around the air sacs is scarred and stiff, so the lungs cannot stretch (restrictive, not obstructive).
    Wrong idea “If the lungs are damaged, FEV₁/FVC must be low.”
    Right idea No. In fibrosis FEV₁/FVC is normal or even high. It is low in obstruction (asthma, COPD).
    Wrong idea “The scarring can be healed with medicine or rest.”
    Right idea No. Scar tissue stays. Antifibrotic medicines can slow the disease; oxygen, rehabilitation and (for some) transplant help in other ways.
    Wrong idea “People with fibrosis breathe slowly and deeply to get more air.”
    Right idea The opposite: stiff lungs make deep breaths hard, so breathing is fast and shallow.
    Wrong idea “A normal oxygen level at rest means the lungs are fine.”
    Right idea Not always. Oxygen can drop only with effort, because the thick wall slows oxygen transfer when blood moves fast, so doctors also test during exercise.
    Wrong idea “Only smokers get pulmonary fibrosis.”
    Right idea No. Dusts, some medicines, radiation, autoimmune disease and genes can cause it, and for many people the cause is unknown. It is not contagious.

    ❓ FAQ

    Concept What is pulmonary fibrosis?►

    Pulmonary fibrosis (PF) is scarring of the lung tissue. Too much collagen builds up in the thin tissue around the air sacs (the interstitium), so the walls become thick and stiff. The scarring is permanent. In idiopathic pulmonary fibrosis (IPF) no cause is found; it mostly affects older adults.

    Key takeaway: PF is permanent scarring that makes the lungs stiff.
    Concept Why do fibrotic lungs take in less air?►

    Scarred lungs are stiff, so they stretch less (low compliance, C = ΔV/ΔP). The breathing muscles must make a much larger pressure change to get the same volume, so each breath is smaller. The total lung capacity and the forced vital capacity are reduced; in this simulator, FVC is about 60% of normal at severity 50.

    Key takeaway: stiffness limits the volume of air the lungs can hold.
    Spirometry What are FVC and FEV1?►

    In spirometry you breathe in as far as you can and blow out as hard and as long as you can. The total volume blown out is the forced vital capacity (FVC). The volume blown out in the first second is FEV1 (forced expiratory volume in 1 second). A healthy adult has an FVC near 4.6 L and an FEV1 near 3.7 L (typical values; they depend on sex, age and height).

    Key takeaway: FVC = how much air; FEV1 = how fast it comes out.
    Spirometry Why is FEV1/FVC normal or high in pulmonary fibrosis but low in asthma or COPD?►

    In fibrosis the airways are open, so the small amount of air that the lungs hold leaves quickly: FEV1 and FVC fall together and the ratio stays about 0.80 or rises to 0.85–0.90. In asthma and COPD the airways are narrowed, so the air leaves slowly, FEV1 falls much more than FVC and the ratio drops below about 0.70.

    Key takeaway: restrictive = small lungs, normal or high ratio; obstructive = low ratio.
    Concept What is lung compliance?►

    Compliance is how easily the lungs stretch: C = change in volume divided by change in pressure (ΔV/ΔP), in liters per cmH2O. Healthy lungs are about 0.20 L/cmH2O in this model. Scarred, stiff lungs have a lower compliance, for example about 0.11 at severity 50.

    Key takeaway: low compliance = stiff lungs.
    Gas exchange Why can the oxygen level fall during exercise even if it is normal at rest?►

    The scarred alveolar wall is thicker, so oxygen crosses more slowly (Fick’s law: rate is about area × pressure difference ÷ thickness). At rest the blood spends about 0.75 s in the capillary, which is enough time. In exercise the blood passes faster and there is not enough time, so the blood oxygen (SpO2) can fall. In this model the values are illustrative.

    Key takeaway: a slow barrier plus fast blood flow means low oxygen during effort.
    Causes What causes pulmonary fibrosis?►

    Known causes and risk factors include long-term exposure to asbestos, silica or coal dust, some medicines (for example bleomycin, amiodarone and nitrofurantoin), radiation to the chest, autoimmune diseases such as rheumatoid arthritis or scleroderma, and hypersensitivity pneumonitis. For many people, the cause is not found (idiopathic). Older age, a history of smoking, reflux and genes are associated with IPF.

    Key takeaway: many causes, and often no known cause.
    Care Can pulmonary fibrosis be cured or reversed?►

    The scarring cannot be reversed. Antifibrotic medicines (pirfenidone and nintedanib) can slow the decline in lung function. Oxygen therapy, pulmonary rehabilitation, vaccination and, for selected patients, a lung transplant are other parts of care. Talk to a doctor: this page is educational and is not medical advice.

    Key takeaway: treatment slows the disease; it does not remove scars.
    About this page How accurate are the numbers in this simulation?►

    The simulator uses approximate textbook values for a typical healthy adult (TV 0.5 L, IRV 3.0 L, ERV 1.1 L, RV 1.2 L, TLC 5.8 L, FEV1/FVC 0.80) and a simple model in which the severity slider sets the FVC as a percentage of normal (mild about 70–80%, moderate 50–69%, severe below 50%). The 3D scarring is drawn in your browser and is not a patient scan, and the oxygen and walk-test values are illustrative. Real people vary a lot.

    Key takeaway: a teaching model, not a diagnosis.