CLIN 512 • Respiratory System

Pulmonary Function Tests

Interactive Mastery Guide

Faculty Directed Study Albert M. Brady, MD, FACP Pacific Northwest University, COM
Progress: 0/11 sections
01

Learning Objectives Dashboard

This table maps every learning objective to a concise key answer. Use it as your roadmap—if you can address each row from memory, you own this material.

# Learning Objective Key Answer
1 Know the indications for performing and ordering pulmonary function tests There are 7 indications: diagnose pulmonary disease, assess asymptomatic smokers, preoperative evaluation in asthma/COPD, monitor occupational exposures, evaluate respiratory disease severity as co-morbidity, medical/legal evaluation of impairment, and evaluate therapeutic drug effects (positive like bronchodilators; negative like Bleomycin).

You cannot diagnose COPD without PFTs.
2 Understand and discuss lung volumes and lung capacities The four key volumes are TLC (total air in lungs), FRC (air remaining after normal expiration), RV (air remaining after forced expiration—cannot be breathed out), and VC (difference between TLC and RV).

RV + VC = TLC.

TLC < 80% predicted indicates restrictive lung disease.
3 Identify and discuss parameters of flow-volume loops Flow-volume loops plot expiratory and inspiratory flow (Y-axis) against volume (X-axis).

The expiratory curve shows a rapid rise to peak flow followed by a nearly linear fall.

The inspiratory curve is a symmetrical saddle shape.

The loop is repeated at least 3 times for reproducibility.
4 Differentiate obstructive vs. restrictive patterns on flow loops, including intra- and extra-thoracic obstructions Obstruction: FEV1/FVC < 70%, with expiratory flow limitation.

Restriction: FEV1 and FVC both decreased proportionately, so FEV1/FVC ratio is preserved.

Fixed upper airway obstruction flattens both limbs; variable extrathoracic flattens the inspiratory limb; variable intrathoracic flattens the expiratory limb.
5 Know the meaning of expiratory flow rate, FEV1, and FEV1/FVC FEV1 is the maximum volume exhaled in the first second of a forced vital capacity maneuver.

FVC is the total volume forcefully exhaled.

FEV1/FVC < 70% defines obstruction.

In restriction, both FEV1 and FVC decrease proportionately, preserving the ratio.
6 Know when to use Diffusion Lung Capacity for Carbon Monoxide (DLCO) DLCO measures gas transfer across the alveolar-capillary membrane using a single 10-second CO inhalation.

It must be ordered separately from PFTs.

DLCO is especially useful in restrictive disease to distinguish intrinsic lung disease (DLCO reduced) from chest wall/neuromuscular causes (DLCO normal).
7 DLCO test details and interpretation Normal DLCO is ≥ 80% predicted (typical range 80–120%).

Low DLCO + obstruction = emphysema.

Low DLCO + restriction = interstitial lung disease.

Low DLCO + normal PFTs = anemia, CHF, early ILD, or pulmonary vascular disease.

Asthma has normal or high DLCO.
8 Know definitions of pulmonary volumes (TLC, TV, etc.) TLC = total air in lungs at max inspiration.

TV = air moved in a normal resting breath.

IRV = extra air inhaled beyond normal inspiration.

ERV = extra air exhaled beyond normal expiration.

RV = air remaining after maximal expiration.

VC = TLC − RV.

FRC = air remaining after normal expiration.
9 Know the GOLD stages of COPD Stage 1 (Very Mild): FEV1 ≥ 80%.

Stage 2 (Moderate): FEV1 50–80%.

Stage 3 (Severe): FEV1 30–50%.

Stage 4 (Very Severe): FEV1 < 30%, or Stage 3 + low O2.

Caution: up to 20% of Stage 1 patients revert to normal; 25% if they stop smoking.
10 Understand the purpose of the methacholine challenge Methacholine challenge is a bronchoprovocation test used to demonstrate hypersensitive (hyperreactive) airways consistent with asthma.

It is indicated when asthma is strongly suspected but PFTs are normal.

The test carries some risk and should be used judiciously.
11 Be familiar with diagnostic procedures in respiratory disease Diagnostic modalities include imaging (chest X-ray, CT/helical CT, MRI, ultrasound, nuclear medicine/V-Q scan, PET scan, virtual bronchoscopy) and tissue-sampling techniques.

CT is superior to plain film for mediastinal disease, emphysema characterization, and lung cancer staging.

MRI excels at vascular assessment without contrast.
Clinical Pearl: This objectives table doubles as an exam checklist. If you can speak to every row without looking, you are board-ready on PFTs.
02

PFT Fundamentals

Three Categories of Respiratory Disease

Obstructive (Most Common)

Disorders primarily of the airways. Characterized by resistance to expiratory airflow.

  • Asthma (reversible)
  • COPD
  • Bronchiectasis
  • Bronchiolitis

Restrictive

Lungs with increased stiffness or reduced expansion capability.

  • Parenchymal lung disease (e.g., pulmonary fibrosis)
  • Chest wall & pleural abnormalities (e.g., kyphoscoliosis)
  • Neuromuscular disease

Vascular

Disorders of the pulmonary vasculature that produce PFT abnormalities.

  • Pulmonary embolism
  • Pulmonary hypertension
  • Pulmonary veno-occlusive disease

Spirometry: The First Test for Shortness of Breath

Spirometry is the initial pulmonary function test to order when a patient presents with shortness of breath because it is readily available in most clinics. Spirometry measures airflow in the tubes and assesses whether flow is obstructive.

Spirometry is a key diagnostic test for asthma and COPD, and is useful in the evaluation of chronic cough and reversible airway etiologies. It can monitor a broad spectrum of respiratory diseases including asthma, COPD, interstitial lung disease, and neuromuscular diseases affecting respiratory muscles.

Spirometry is an effort-dependent test. A diminished FEV1/FVC (often defined as < 70% predicted) is diagnostic of obstruction. The flow-volume loop, by contrast, is effort-independent.

Seven Indications for Pulmonary Function Tests

# Indication Detail
1 Diagnose pulmonary disease Establish the presence and type of pulmonary dysfunction
2 Assess lung function in asymptomatic smokers Detect clinically silent airflow limitation before symptoms appear
3 Preoperative evaluation in asthma/COPD Quantify reversible airway disease risk before surgery
4 Monitor occupational lung exposures Track progressive decline from workplace inhalants
5 Evaluate severity of respiratory disease as co-morbidity Assess pulmonary impact of other diseases such as autoimmune conditions
6 Medical/legal evaluation of impairment or disability Objective documentation for disability and legal proceedings
7 Evaluate therapeutic drug effects Positive effects (bronchodilators) and negative effects (e.g., Bleomycin pulmonary toxicity)
You cannot diagnose COPD without PFTs. This is a testable, absolute statement from the professor.

Five Challenges & Pitfalls of PFTs

# Pitfall Explanation
1 Very operator dependent Requires a conscientious respiratory technologist, nurse, or physician to obtain valid results.
2 Very dependent on patient effort You rely on feedback from the respiratory technologist regarding the patient's effort and cooperation.
3 Results compared to ATS predicted values All test normals are adjusted for age, gender, height, and ethnicity using American Thoracic Society standards.
4 Must be reproducible At least 3 attempts are obtained. Reproducible numbers signify good patient effort.
5 Caution with single-spirometry COPD diagnosis Up to 20% of GOLD Stage 1 patients revert to normal. If they stop smoking, 25% will revert to normal.
Clinical Pearl: PFTs are both operator-dependent and patient effort-dependent. Always check the technologist's comments on patient cooperation before interpreting results. Reproducibility across at least 3 attempts is required for valid data.

Test Your Knowledge

What is the single most important initial test to order for a patient presenting with shortness of breath?

Spirometry—it is readily available in most clinics and assesses for obstructive pathophysiology.

Name the 3 categories of respiratory disease.

Obstructive lung diseases (most common), restrictive disorders, and abnormalities of the pulmonary vasculature.

Why should you be cautious diagnosing COPD from a single spirometry test?

Up to 20% of GOLD Stage 1 patients revert to normal on subsequent testing. If they stop smoking, 25% will revert to normal.

What four factors are used to adjust PFT predicted values?

Age, gender, height, and ethnicity (based on American Thoracic Society standards).

03

Lung Volumes & Capacities

Key Diagrams

Spirogram demonstrating a slow vital capacity maneuver and various lung volumes, including TLC, VC, FRC, RV, TV, IRV, and ERV - FIGURE 306e-2
FIGURE 306e-2: Spirogram demonstrating a slow vital capacity maneuver and various lung volumes. YOU MUST KNOW THIS FIGURE.
Diagram showing lung volumes and capacities with labeled compartments including TLC, VC, IC, FRC, ERV, TV, IRV, and RV
Lung volumes and capacities
The Essentials of spirometry showing tidal volume as normal resting breathing, vital capacity as maximal inhalation to maximal exhalation, and residual volume as the air that cannot be exhaled
Spirometry essentials: Tidal volume is normal resting inspiration and expiration. Vital capacity is easily measured. RV is estimated.

Volume & Capacity Definitions

TLC — Total Lung Capacity
The total volume of air contained in the lungs at maximum inspiration. Determined by the ability of the inspiratory pump (brain, nerves, muscles) to expand the chest wall against the lung's tendency to recoil inward.
FRC — Functional Residual Capacity
The volume of air remaining in the lungs at the end of normal expiration. It is the relaxation volume. Not a reliable measurement in obstructive disease—FRC may be elevated, imposing extra load on inspiratory muscles and leading to fatigue.
RV — Residual Volume
The volume of air remaining in the lungs after maximal forced expiration. This air cannot be breathed out. Determining RV requires special testing: Helium dilution, Nitrogen washout, or body plethysmography.
VC — Vital Capacity
The difference between TLC and RV. Represents the maximum volume of air that can be exhaled after a maximal inhalation. VC = TLC − RV.
TV — Tidal Volume
The volume of air moved in and out of the lungs during a normal resting breath. It is the baseline breathing volume.
IRV — Inspiratory Reserve Volume
The additional volume of air that can be inhaled beyond a normal tidal inspiration. Represents the reserve capacity above normal breathing.
ERV — Expiratory Reserve Volume
The additional volume of air that can be forcefully exhaled beyond the end of a normal tidal expiration. Represents the reserve below normal breathing but above RV.

Key Relationships

RV + VC = TLC
TLC < 80% predicted = Restrictive Lung Disease

How TLC Changes in Disease

Decreased TLC (Restriction)

  • Neuromuscular disease — inspiratory pump failure reduces expansion
  • Severe kyphoscoliosis — chest wall deformity limits expansion
  • Pulmonary fibrosis — increased inward recoil of lung parenchyma

Increased TLC (Hyperinflation)

  • Emphysema — decreased inward recoil leads to hyperinflation and air trapping, resulting in increased TLC

How RV Is Determined

Young & Healthy Individuals

RV is determined by a competition between the strength of expiratory muscles and the compressibility of the chest wall.

Middle Age / Obstructive Disease

RV is determined by flow limitation: expiratory flow rates at low lung volumes are so low that expiration is prolonged and not completed before the subject takes another breath.

Clinical Pearl: RV requires special testing (He dilution, N2 washout, or body plethysmography) because it cannot be measured by simple spirometry—you cannot breathe out the residual volume. Body plethysmography is the gold standard for lung volume measurement.

FRC in Obstructive Disease

In patients with obstructive lung disease, FRC may be elevated. This imposes a significant extra load on the inspiratory muscles, which can result in muscle fatigue. FRC is the relaxation volume at the end of expiration, and it is not a reliable measurement in the setting of obstruction.

Test Your Knowledge

What equation relates the three major lung compartments?

RV + VC = TLC. Vital capacity is the difference between total lung capacity and residual volume.

Why does emphysema increase TLC while pulmonary fibrosis decreases it?

Emphysema decreases inward recoil of the lung, leading to hyperinflation and air trapping (increased TLC). Pulmonary fibrosis increases inward recoil, pulling the lung to a smaller volume (decreased TLC).

Name the three methods used to determine residual volume.

Helium dilution, Nitrogen washout, and body plethysmography (gold standard). Simple spirometry cannot measure RV.

What TLC threshold defines restrictive lung disease?

TLC < 80% of predicted value defines restrictive lung disease.

04

Airflow & Spirometry

Physics of Airflow

Air flows through a tube when there is a pressure difference between the ends—just like blood flow. In the respiratory system, the pressure difference exists between alveolar pressure and the mouth.

Laminar Flow

Smooth, orderly flow through airways. Depends on the characteristics of the gas and the tube through which it travels.

Turbulent Flow

Chaotic, disordered flow. More likely in larger airways and at higher flow rates.

Airway Resistance

Most resistance to airflow occurs in the first few divisions of the airways. The more distal airway divisions have a large cross-sectional area and therefore contribute less resistance to airflow.

Resistance is not constant across all lung volumes:

  • High lung volumes: lungs expand, airways enlarge, resistance decreases
  • Low lung volumes: airways narrow, resistance increases

Other Factors That Increase Airway Resistance

  • Smooth muscle constriction — bronchoconstriction narrows airway lumen
  • Secretions in the airways — mucus plugging reduces available lumen
  • Edema in the airway wall — swelling encroaches on the lumen
  • Loss of tethering (emphysema) — small airways that are normally held open during expiration collapse, increasing resistance to expiratory airflow
Clinical Pearl: Obstructive lung diseases are characterized by resistance to expiratory flow. This is the defining feature—the problem is getting air out, not in.

Four Categories of PFT Information

# Category What It Measures
1 Lung Volumes Maximum volume of the lungs and its sub-compartments (TLC, RV, FRC, etc.)
2 Flow Rates Maximum flow of gas out of and into the lungs (FEV1, FVC, peak flow)
3 Diffusing Capacity Transfer of gas from the alveolar space into the capillary blood stream (DLCO)
4 Maximal Inspiratory/Expiratory Pressures Applied strength of the respiratory muscles (MIP/MEP)

Key Spirometric Measurements

FEV1 — Forced Expiratory Volume in 1 Second
The maximum volume of air that can be exhaled during the first second of a forced vital capacity (FVC) maneuver. In obstruction, FEV1 is reduced more than FVC. FEV1 is the single most important number for grading severity of obstruction (used in GOLD staging).
FVC — Forced Vital Capacity
The total volume of air that can be forcefully exhaled after maximal inhalation. In obstruction, FVC may be reduced but less than FEV1. In restriction, both FEV1 and FVC decrease proportionately, preserving the FEV1/FVC ratio.
Clinical Pearl: FEV1/FVC < 70% defines obstruction. This is the single most important ratio in all of PFT interpretation. In restrictive disease, both FEV1 and FVC decrease proportionately, so the FEV1/FVC ratio is preserved (normal or even elevated).

Spirometry vs. Flow-Volume Loop

Spirometry

  • Effort-dependent
  • Measures FEV1, FVC, and their ratio
  • Key diagnostic test for asthma and COPD
  • Requires good patient cooperation
  • At least 3 reproducible attempts required

Flow-Volume Loop

  • Effort-independent
  • Plots flow (Y-axis) against volume (X-axis)
  • Visualizes expiratory flow rates
  • Detects upper airway obstructions not seen on standard FVC
  • Shows response to bronchodilator therapy
  • Used in methacholine challenge testing
The clinician should always examine the flow-volume loop in addition to the FEV1/FVC ratio. Upper airway obstruction (pharynx, larynx, trachea) is usually impossible to detect from standard FVC maneuvers alone.

Test Your Knowledge

Where does most airway resistance occur—proximal or distal airways?

In the first few divisions of the airways (proximal). Distal airways have a large cross-sectional area and contribute less resistance.

What FEV1/FVC ratio defines airflow obstruction?

FEV1/FVC < 70% of predicted value defines obstruction.

Why is the flow-volume loop important even when spirometry numbers look normal?

Upper airway obstruction (pharynx, larynx, trachea) is usually impossible to detect from standard FVC maneuvers alone. The flow-volume loop can reveal fixed or variable upper airway obstructions that spirometry misses.

Name the four categories of information obtainable from routine PFTs.

1) Lung volumes (max volume and sub-compartments), 2) Flow rates (max flow in and out), 3) Diffusing capacity (gas transfer from alveoli to capillaries), 4) Maximal inspiratory/expiratory pressures (respiratory muscle strength).

05

Flow-Volume Loops

What Is a Flow-Volume Loop?

A flow-volume loop is the expiratory and inspiratory flow plotted against volume during a forced breathing maneuver. It provides a visual representation of airflow dynamics throughout the entire breathing cycle and is effort-independent, making it a powerful complement to standard spirometry.

X Axis
Volume (liters)
Y Axis
Flow (liters per second)
Expiratory Limb
Upper portion of the loop (above the x-axis); flow is plotted as positive
Inspiratory Limb
Lower portion of the loop (below the x-axis); flow is plotted as negative

Normal Loop Anatomy

A normal flow-volume loop has a characteristic shape that you must recognize instantly:

  • Expiratory limb: Rapid rise to peak expiratory flow rate (PEFR), followed by a nearly linear fall in flow back to zero as the lungs empty. A well-defined peak indicates good initial patient effort.
  • Inspiratory limb: A relatively symmetrical, saddle-shaped curve below the x-axis. The inspiratory flow is more uniform throughout the maneuver.
Clinical Pearl: The slightly concave appearance of the expiratory portion of the curve is normal with aging alone. However, in a 20-year-old, that same concave pattern would indicate the presence of airflow obstruction. Context matters when reading flow-volume loops.
Spirometric flow-volume curve showing peak flow and volume-time relationship
Spirometric Flow-Volume (Panel A) and Volume-Time (Panel B) Curves for a Healthy 52-Year-Old Man
Normal flow-volume loop with lung volumes labeled showing FEV1, PEFR, FEF points, and relationship to IRV, Vt, ERV, RV
Flow-volume loop with lung volumes and capacities. The patient starts expiration at the red arrow as hard and fast as they can, continues until done, then takes as big a breath as possible. Repeated 3 times for reproducibility.

The Maneuver

The patient begins at the red arrow by exhaling as hard and as fast as they can. This continues until they can blow no more, then they take as big a breath in as hard and as fast as they can. This completes the loop. The maneuver is typically repeated 3 times to ensure reproducible results.

Ordering a pulmonary function study will produce flow-volume loops with associated patient numbers and ratios compared to normal, along with lung volumes.

When to Order Flow-Volume Loops

  • Stridor heard over the neck — suggests upper airway pathology
  • Unexplained dyspnea — especially when standard spirometry is unrevealing
Clinical Pearl: Standard FVC maneuvers CANNOT detect upper airway obstruction (pharynx, larynx, or trachea). The flow-volume loop is essential for identifying these lesions. If you only order standard spirometry, you will miss upper airway pathology.

Uses of Flow-Volume Loops

  • Visualize expiratory flow rates — see the shape and magnitude of airflow throughout expiration
  • Assess response to bronchodilator therapy — compare pre- and post-bronchodilator loops
  • Response to bronchoprovocation (methacholine challenge) — demonstrates hypersensitive airways in suspected asthma

Upper Airway Obstruction Patterns

There are four classic flow-volume loop patterns you must recognize. These patterns arise from the mechanical relationship between airway pressure and the location/nature of the obstruction.

Four flow-volume loop patterns: A) Normal B) Fixed obstruction C) Variable extrathoracic D) Variable intrathoracic
Flow-volume loops in upper airway obstruction: (A) Normal (B) Fixed (C) Variable extrathoracic (D) Variable intrathoracic

(A) Normal

  • Rapid rise to peak expiratory flow
  • Nearly linear fall in expiratory flow
  • Saddle-shaped, symmetrical inspiratory curve
  • No flattening on either limb

(B) Fixed Obstruction

  • Can be intrathoracic OR extrathoracic
  • Flattening on BOTH inspiratory AND expiratory limbs
  • Flow is limited in both directions equally
  • Example: tracheal stenosis

(C) Variable Extrathoracic

  • Flattening on INSPIRATORY limb only
  • Expiratory limb appears normal
  • During inspiration, negative pressure sucks the softened or obstructed extrathoracic airway inward
  • During expiration, positive pressure pushes it open
  • Examples: tracheomalacia, vocal cord paralysis

(D) Variable Intrathoracic

  • Flattening on EXPIRATORY limb only
  • Inspiratory limb appears normal
  • During expiration, positive intrathoracic pressure compresses the airway at the obstruction site
  • During inspiration, negative pressure pulls the airway open
  • Example: intrathoracic tracheal tumor
Extrathoracic upper airway obstruction flow-volume loop showing inspiratory flattening
Extrathoracic obstruction: during inspiration the softened trachea is sucked inward causing partial collapse. Expiratory pressure is high enough to push trachea open.
Clinical Pearl: Tracheomalacia is a softening of the tracheal cartilage, classically after prolonged intubation (though it can occur in patients who have never been intubated). The key mechanism: during inspiration, negative pressure sucks the softened trachea inward causing partial collapse. During expiration, positive pressure pushes it open. This produces flattening on the inspiratory limb only (variable extrathoracic pattern).
Memory aid: Fixed = Both limbs affected. Variable extrathoracic = Inspiratory flattening. Variable intrathoracic = Expiratory flattening. Tracheal stenosis is a FIXED lesion → present on BOTH sides of the loop.

Test Your Knowledge

A patient presents with stridor after prolonged ICU intubation. Their flow-volume loop shows flattening on the inspiratory limb only, with a normal expiratory limb. What is the most likely diagnosis, and what type of obstruction pattern is this?

This is a variable extrathoracic obstruction pattern, most consistent with tracheomalacia. Prolonged intubation softened the tracheal cartilage. During inspiration, negative pressure sucks the weakened trachea inward (partial collapse); during expiration, positive pressure pushes it open, so only the inspiratory limb is affected.

A flow-volume loop shows flattening on BOTH the inspiratory and expiratory limbs. What type of obstruction is this, and what is a classic example?

This is a fixed upper airway obstruction pattern. A classic example is tracheal stenosis. Because the lesion is rigid and fixed, it limits flow equally in both directions regardless of airway pressure changes during the respiratory cycle.

A 52-year-old man's flow-volume loop shows a slightly concave expiratory curve. A 20-year-old woman has the same pattern. How do you interpret each?

In the 52-year-old, a slightly concave expiratory curve is a normal age-related change. In the 20-year-old, the same pattern is abnormal and suggests airflow obstruction. Always interpret flow-volume loop shape in the context of the patient's age.

Why can't standard FVC spirometry detect a pharyngeal or tracheal obstruction? What test should you order instead?

Standard FVC maneuvers measure overall airflow and volumes but cannot localize obstruction to the upper airways (pharynx, larynx, trachea). A flow-volume loop is needed because it displays the shape of both inspiratory and expiratory flow, revealing characteristic flattening patterns that pinpoint upper airway obstruction and distinguish fixed from variable lesions.

06

Obstructive vs Restrictive Disease

The Two Major PFT Patterns

Respiratory diseases fall into two fundamental physiologic categories based on pulmonary function testing. Recognizing which pattern is present is the first and most critical step in PFT interpretation.

Obstructive Disease

Difficulty getting air out. Airways are narrowed, collapsed, or plugged. Airflow is limited during expiration. The hallmark is a reduced FEV1/FVC ratio.

Examples: Asthma, COPD (emphysema and chronic bronchitis), bronchiectasis, bronchiolitis

Restrictive Disease

Difficulty getting air in. Lungs cannot fully expand due to stiff parenchyma, chest wall problems, or weak muscles. The hallmark is a reduced TLC.

Examples: Pulmonary fibrosis, kyphoscoliosis, neuromuscular disease, obesity, pleural disease

Comprehensive Comparison Table

Parameter Obstructive Restrictive
FEV1 Decreased (more than FVC) Decreased
FVC Decreased (less than FEV1) Decreased
FEV1/FVC Ratio < 70% — DECREASED Normal or increased — PRESERVED
TLC Normal or increased (hyperinflation) < 80% predicted — DECREASED
RV Increased (air trapping) Decreased
DLCO Low in emphysema; Normal or high in asthma Low in ILD; Normal in chest wall/neuromuscular disease
Flow-Volume Loop Scooped/concave expiratory limb Smaller but preserved normal shape
Examples Asthma, COPD, bronchiectasis, bronchiolitis Pulmonary fibrosis, kyphoscoliosis, neuromuscular disease, obesity, pleural disease

Key Diagnostic Criteria

Clinical Pearl: FEV1/FVC < 70% = OBSTRUCTION. This is the single most important ratio in PFT interpretation. In obstruction, ALL expiratory flows are reduced, but FEV1 falls more than FVC, which is why the ratio drops.
Clinical Pearl: TLC < 80% predicted = RESTRICTION. You cannot diagnose restrictive disease from spirometry alone — you need lung volumes. A low FVC on spirometry suggests restriction but does not confirm it (FVC can also be low in obstruction due to air trapping).
Clinical Pearl: Body plethysmography is the gold standard for measuring lung volumes. The patient is placed in a closed, sealed chamber, and lung volumes are calculated from pressure changes. This is how you definitively confirm restrictive physiology.

Expiratory Flow Mechanics

In Obstruction

ALL expiratory flows are reduced, but FEV1 decreases MORE than FVC. This disproportionate reduction is what drives the FEV1/FVC ratio below 70%. The flow-volume loop shows a characteristic scooped or concave expiratory limb, reflecting progressive airflow limitation as the lungs empty.

In Restriction

FEV1 and FVC are each decreased, but they decrease proportionately. Because both numerator and denominator fall together, the FEV1/FVC ratio is preserved (normal or even increased). The flow-volume loop is smaller overall but retains its normal shape.

Visual Pattern Recognition

Flow-volume loops comparing obstructive and restrictive patterns
Contrasting obstructive and restrictive flow-volume loop patterns
Restrictive pattern flow-volume loop
Restrictive pattern on flow-volume loop
Common abnormalities of pulmonary function showing pulmonary fibrosis, obesity, myasthenia gravis, acute asthma, and severe emphysema with values and flow-volume loops
Common abnormalities of pulmonary function. Values expressed as percentage of predicted. Shows typical flow-volume loop configurations for each condition.
PFT interpretation data showing additional pulmonary function values and patterns
PFT interpretation data
PFT interpretation data with clinical correlations and reference values
PFT interpretation data

Test Your Knowledge

A patient's PFTs show: FEV1 55% predicted, FVC 80% predicted, FEV1/FVC = 52%. Is this obstructive, restrictive, or both? Explain why.

This is an obstructive pattern. The FEV1/FVC ratio is 52%, which is well below 70%. Notice that FEV1 is reduced much more than FVC — this disproportionate reduction is the hallmark of obstruction. FEV1 fell more because air trapping and airway narrowing specifically limit expiratory flow rates.

A patient's PFTs show: FEV1 60% predicted, FVC 58% predicted, FEV1/FVC = 85%, TLC = 65% predicted. What is the pattern?

This is a restrictive pattern. The FEV1/FVC ratio is 85% (preserved — well above 70%), but TLC is 65% (< 80% predicted), confirming restriction. Both FEV1 and FVC are reduced proportionately, which is why the ratio stays normal. The low TLC clinches the diagnosis.

Why can't you diagnose restrictive lung disease from spirometry alone? What additional test do you need?

Spirometry measures FEV1, FVC, and their ratio, but it does not measure total lung capacity (TLC). A low FVC on spirometry may suggest restriction, but it can also occur in obstruction due to air trapping. You need lung volume measurement (ideally by body plethysmography, the gold standard) to confirm TLC < 80% predicted and definitively diagnose restriction.

A patient with severe emphysema has PFTs. Predict what you'd see for: FEV1/FVC, TLC, RV, DLCO, and flow-volume loop shape.

FEV1/FVC: Decreased (< 70%) due to obstruction. TLC: Increased (hyperinflation from loss of elastic recoil). RV: Increased (air trapping — air can't be fully exhaled). DLCO: Low (destruction of alveolar-capillary surface reduces gas transfer). Flow-volume loop: Scooped/concave expiratory limb with reduced peak flow and prolonged expiration.

07

DLCO — Diffusing Capacity

What Is DLCO?

Full Name
Diffusion Lung Capacity utilizing Carbon Monoxide
What It Measures
The ability of carbon monoxide (CO) to cross the alveolar-capillary membrane — a surrogate for how well gases transfer between alveoli and blood
How It Works
Patient takes a single breath of CO and holds for 10 seconds. The amount of CO absorbed is measured. Better diffusing capacity = more CO absorbed.
Normal Range
80–120% of predicted (typical; some lab variation in upper limit)
Abnormal
< 80% of predicted

Practical Considerations

  • Equipment: The DLCO instrument is very expensive and requires regular biomedical engineering maintenance and calibration. Equipment and trained personnel are usually found only in large hospitals and specialized centers.
  • Ordering: DLCO must be ordered separately from PFTs. If you order PFTs, it will NOT include a DLCO. You must specifically request it.
A reduced DLCO implies a loss of effective capillary surface and interface. This can include thickening of the alveolar membrane (as with drug-induced inflammation) or alternatively, pulmonary edema. Destruction of alveolar walls (emphysema) also reduces the available surface area for gas exchange.

The Big 3 — High-Yield DLCO Pearls

These three associations are among the most testable concepts in pulmonary medicine. Commit them to memory:

Clinical Pearl: Low DLCO + OBSTRUCTION → Think EMPHYSEMA. Destruction of alveolar walls eliminates capillary surface area, reducing gas transfer. This distinguishes emphysema from asthma and chronic bronchitis, which are also obstructive but have normal or high DLCO.
Clinical Pearl: Low DLCO + RESTRICTION → Think INTERSTITIAL LUNG DISEASE. Fibrosis and inflammation thicken the alveolar-capillary membrane, impairing diffusion. This distinguishes ILD from other causes of restriction (chest wall, neuromuscular) where the membrane is intact.
Clinical Pearl: Low DLCO + NORMAL PFTs (in isolation) → Think ANEMIA, CHF, INTERSTITIAL LUNG DISEASE, or PULMONARY VASCULAR DISEASE. An isolated low DLCO with otherwise normal spirometry and lung volumes is a red flag for systemic or vascular processes affecting gas exchange.

DLCO in Specific Diseases

Clinical Context DLCO Finding Interpretation
Emphysema (COPD) Low Alveolar wall destruction reduces capillary surface area; lower DLCO = more lung involvement
Asthma Normal or High Airways are inflamed/constricted but alveolar-capillary membrane is intact; obstructive pattern with preserved DLCO
Interstitial Lung Disease Low Fibrosis thickens the alveolar membrane, impairing gas transfer
Kyphoscoliosis Normal Restriction from chest wall deformity; lung parenchyma and membrane are normal
Neuromuscular Disease Normal Restriction from weak respiratory muscles; membrane is intact
Obesity Normal Restriction from mechanical loading; lung tissue itself is normal
Pleural Effusion / Thickening Normal Restriction from pleural disease; alveolar-capillary interface is unaffected
Anemia Low Fewer hemoglobin molecules available to bind CO, even though the membrane is normal
CHF / Pulmonary Edema Low Fluid in the interstitium increases diffusion distance across the membrane
Pulmonary Vascular Disease Low Loss of pulmonary capillary bed reduces available surface for gas exchange

DLCO as a Differentiator in Restrictive Disease

DLCO is extremely valuable when you've already identified restrictive physiology (reduced VC + reduced TLC). The DLCO tells you why the lungs are restricted:

Low DLCO → Intrinsic Lung Disease

  • Interstitial lung disease (pulmonary fibrosis)
  • The parenchyma itself is diseased
  • Thickened or destroyed alveolar-capillary membrane

Normal DLCO → Extrinsic Restriction

  • Kyphoscoliosis
  • Neuromuscular disease
  • Obesity
  • Pleural effusion or thickening
  • The lung tissue itself is healthy
Clinical reasoning chain: Flow-volume loop shows reduced VC + lung volumes confirm reduced TLC → restrictive disease confirmed. Then check DLCO: if low → interstitial lung disease. If normal → chest wall, neuromuscular, obesity, or pleural cause.

When to Order DLCO

  • Any patient with confirmed restrictive physiology on lung volumes — to distinguish intrinsic lung disease from other causes
  • Suspected emphysema in a smoker with obstructive PFTs — a low DLCO confirms parenchymal destruction and quantifies severity
  • Unexplained dyspnea with normal spirometry and lung volumes — an isolated low DLCO may reveal anemia, early ILD, CHF, or pulmonary vascular disease
  • Monitoring drug-induced lung toxicity (e.g., bleomycin) — DLCO drops before symptoms appear
  • Evaluating smokers with COPD — the lower the DLCO, the more lung involvement anatomically

Test Your Knowledge

A patient has obstructive PFTs (FEV1/FVC = 58%) and a normal DLCO. Another patient has the same FEV1/FVC but a DLCO of 45% predicted. What diagnoses should you consider for each?

Normal DLCO + obstruction: Think asthma (or chronic bronchitis). The airways are constricted but the alveolar-capillary membrane is intact. Low DLCO + obstruction: Think emphysema. Alveolar wall destruction has eliminated capillary surface area, reducing gas transfer. DLCO is the key differentiator between these obstructive diseases.

You order PFTs on a patient with suspected pulmonary fibrosis. The spirometry and lung volumes confirm restriction (TLC 62% predicted). Do you have enough information to confirm ILD? What else do you need?

No — restriction alone does not confirm ILD. You need a DLCO, which must be ordered separately from PFTs. If DLCO is low, this supports intrinsic lung disease (ILD). If DLCO is normal, you should consider extrinsic causes of restriction: kyphoscoliosis, neuromuscular disease, obesity, or pleural disease.

A patient has completely normal spirometry and lung volumes, but their DLCO comes back at 55% predicted. What conditions should you consider?

An isolated low DLCO with normal PFTs should prompt consideration of: anemia (fewer hemoglobin molecules to bind CO), congestive heart failure (interstitial edema increases diffusion distance), early interstitial lung disease (DLCO may drop before volumes change), or pulmonary vascular disease (loss of capillary bed). Check a CBC, BNP, and consider CT chest.

Why is DLCO normal or high in asthma but low in emphysema, when both are obstructive diseases?

In asthma, the pathology is airway inflammation and bronchoconstriction — the alveolar-capillary membrane is intact. DLCO may even be slightly elevated due to increased pulmonary blood volume. In emphysema, the pathology is destruction of alveolar walls, which eliminates the capillary surface area where gas exchange occurs. Less surface area = less CO absorbed = low DLCO.

08

GOLD Stages of COPD

Staging COPD by Severity

The Global Initiative for Chronic Obstructive Lung Disease (GOLD) classifies COPD severity based on post-bronchodilator FEV1 as a percentage of predicted. Before staging, you must first confirm the diagnosis.

FEV1/FVC < 70% must be present FIRST to diagnose COPD. Only THEN do you use FEV1 (% predicted) to determine the GOLD stage. You cannot stage COPD without first confirming obstruction.

The Four GOLD Stages

GOLD Stage Severity FEV1 (% Predicted) Key Features
Stage 1 Very Mild ≥ 80% Often asymptomatic; may not know they have COPD; high reversion rate
Stage 2 Moderate 50–80% Dyspnea on exertion; patients typically seek medical attention at this stage
Stage 3 Severe 30–50% Significant dyspnea; frequent exacerbations; reduced quality of life
Stage 4 Very Severe < 30%, or Stage 3 FEV1 + low blood oxygen levels Severe impairment; may qualify for oxygen therapy; cor pulmonale risk
Clinical Pearl: Be cautious about diagnosing COPD from one spirometry. GOLD Stage 1 patients have up to a 20% reversion to normal on repeat testing. If they stop smoking, 25% will revert to normal and lose the diagnosis entirely. Repeat testing is important before labeling a patient with a lifelong diagnosis.

Diagnostic Approach: When to Order What

SOB or Chronic Cough
Order spirometry as the initial test
Suspected Asthma
Order pre- and post-bronchodilator spirometry to demonstrate reversibility
Normal PFT but High Suspicion for Asthma
Order methacholine challenge — demonstrates airway hyperreactivity in patients with normal baseline spirometry
Suspected Restriction
Order lung volumes (body plethysmography) to confirm TLC < 80%, then DLCO to differentiate cause

Methacholine Challenge

The methacholine challenge is a bronchoprovocation test used when asthma is highly suspected but PFTs are normal. Methacholine is a cholinergic agonist that causes bronchoconstriction in patients with hyperreactive airways.

  • Indication: Normal baseline PFT + high clinical suspicion for asthma
  • Mechanism: Inhaled methacholine provokes bronchospasm in hypersensitive airways at doses that would not affect normal airways
  • Positive test: A 20% or greater drop in FEV1 from baseline (PC20) at a low methacholine concentration
  • Risk: The test does carry some risk — it intentionally induces bronchospasm, so bronchodilator rescue must be available
Clinical Pearl: The methacholine challenge is highly sensitive for asthma — a negative test essentially rules it out. However, a positive test is not perfectly specific, as airway hyperreactivity can also be seen in COPD, allergic rhinitis, and post-viral states.

Test Your Knowledge

A patient has an FEV1 of 72% predicted and an FEV1/FVC of 74%. Can you diagnose and stage COPD?

No. You cannot diagnose COPD because the FEV1/FVC ratio is 74%, which is above the 70% threshold. Without confirmed obstruction (FEV1/FVC < 70%), COPD cannot be diagnosed and staging is not applicable, regardless of the FEV1 value.

A patient has FEV1/FVC = 62% and FEV1 = 45% predicted. What GOLD stage is this? What if their blood oxygen is also chronically low?

FEV1/FVC < 70% confirms obstruction (COPD). FEV1 of 45% falls between 30–50%, so this is GOLD Stage 3 (Severe). However, if this patient also has chronically low blood oxygen levels, they would be reclassified as GOLD Stage 4 (Very Severe), since Stage 4 includes patients with Stage 3 FEV1 values plus hypoxemia.

A 45-year-old nonsmoker presents with episodic wheezing and chest tightness. Spirometry is completely normal. What should you order next and why?

Order a methacholine challenge. This patient has classic symptoms of asthma but normal baseline PFTs. The methacholine challenge will provoke bronchospasm in hyperreactive airways, demonstrating the asthma that is not apparent at baseline. A positive test (drop in FEV1 ≥ 20%) supports the diagnosis. Remember this test carries some risk since it intentionally induces bronchoconstriction.

VR

Visual Reference Diagrams

Interactive SVG diagrams for pattern recognition and clinical reasoning

PFT Interpretation Algorithm

Clinical decision pathway from spirometry to diagnosis

Patient presents with SOB, cough, or wheezing
Order SpirometryMeasure FEV1, FVC, and FEV1/FVC ratio
FEV1/FVC < 70%?The defining question for obstruction
YES ↓NO ↓
Obstructive Pathway

FEV1/FVC < 70% — airflow limitation confirmed. FEV1 decreases more than FVC.

Step 1: Pre / Post Bronchodilator Testing
Administer SABA, repeat spirometry in 15 min. Check if FEV1 improves ≥12% AND ≥200 mL.
REVERSIBLE ASTHMA Reversible airflow obstruction. DLCO is normal or high.
NOT REVERSIBLE COPD Fixed airflow obstruction. Classify by GOLD stage below.
GOLD Staging (by FEV1 % predicted)
After confirming COPD (FEV1/FVC < 70%), stage severity using FEV1 alone.
I — Very Mild
FEV1 ≥ 80%
II — Moderate
FEV1 50–80%
III — Severe
FEV1 30–50%
IV — Very Severe
FEV1 < 30%
Step 2: Order DLCO
Differentiates emphysema from asthma/chronic bronchitis in obstructive patients.
DLCO LOW EMPHYSEMA Alveolar wall destruction reduces gas exchange surface area.
DLCO NORMAL/HIGH ASTHMA Alveolar-capillary membrane intact. Airways are the problem, not parenchyma.
Restrictive Pathway

FEV1/FVC is normal or increased, but FVC is decreased — suggesting restriction. Need lung volumes to confirm.

Step 1: Order Lung Volumes
Body plethysmography (gold standard), helium dilution, or nitrogen washout to measure TLC.
TLC < 80% RESTRICTIVE CONFIRMED Lungs cannot fully expand. Proceed to DLCO.
TLC NORMAL NONSPECIFIC PATTERN Low FVC with normal TLC may indicate air trapping, poor effort, or obesity.
Step 2: Order DLCO (if restrictive confirmed)
DLCO distinguishes intrinsic lung disease from extrinsic causes of restriction.
DLCO LOW INTERSTITIAL LUNG DISEASE Thickened alveolar membrane impedes gas diffusion (fibrosis, drug-induced).
DLCO NORMAL EXTRAPULMONARY CAUSE Chest wall (kyphoscoliosis), neuromuscular, obesity, or pleural disease.
Normal Spirometry Pathway

FEV1/FVC and FVC both within normal limits. Spirometry does not show obstruction or restriction.

Clinical Suspicion for Asthma?
If symptoms strongly suggest asthma despite normal PFTs, consider bronchoprovocation.
YES — SUSPECT ASTHMA METHACHOLINE CHALLENGE Demonstrates airway hyperresponsiveness. Carries some risk.
POSITIVE ASTHMA CONFIRMED
NEGATIVE ASTHMA UNLIKELY High negative predictive value. Consider other diagnoses.
NO SUSPICION REASSESS CLINICALLY Consider cardiac, deconditioning, upper airway, or anxiety causes.
Remember: FEV1/FVC < 70% = Obstruction  |  TLC < 80% = Restriction  |  DLCO separates emphysema from asthma  |  DLCO ordered SEPARATELY

Additional SVG Diagrams

Lung Volumes and Capacities Spirogram A spirogram trace showing tidal breathing followed by maximal inspiration and expiration, with labeled lung volumes (TV, IRV, ERV, RV) and capacities (VC, TLC, FRC, IC). Lung Volumes & Capacities — Spirogram 6 5 4 3 2 1 0 Volume (L) Time TV ~0.5L IRV ~3.0L ERV ~1.0L RV ~1.2L (unmeasured) VC TLC IC FRC Tidal breathing Max inspiration Max expiration Tidal breathing Volumes Capacities RV (not measured by spirometry)
Flow-Volume Loop Comparison Four flow-volume loops comparing Normal, Obstructive, Restrictive, and Fixed Upper Airway Obstruction patterns. A faint normal loop is overlaid on abnormal patterns for reference. Flow-Volume Loop Patterns A) Normal Volume (L) Flow (L/s) Exp Insp PEF B) Obstructive Volume (L) scooped C) Restrictive Volume (L) ↓ volume D) Fixed Upper Airway Obstruction Volume (L) plateau plateau Normal reference (ghost) Pattern overlay
DLCO Decision Tree A clinical decision tree for interpreting DLCO results in the context of PFT patterns, branching to diagnoses like emphysema, interstitial lung disease, asthma, and pulmonary vascular disease. DLCO Interpretation — Decision Tree Low DLCO? <80% predicted Yes Check PFT Pattern Obstruction? Yes EMPHYSEMA Parenchymal destruction Restriction? Yes INTERSTITIAL LUNG DISEASE Normal PFTs? Yes Think: Anemia, CHF, early ILD, Pulm Vascular Disease No Normal DLCO With Obstruction? Yes ASTHMA Preserved gas exchange No Normal Key Differentiator DLCO separates emphysema from asthma
PFT Interpretation Algorithm A comprehensive clinical decision flowchart for interpreting pulmonary function tests, from initial spirometry through obstructive and restrictive pattern evaluation to specific diagnoses. PFT Interpretation Algorithm Patient with SOB / Cough Order Spirometry FEV1/FVC < 70%? (or < LLN) Yes OBSTRUCTIVE Pre/Post Bronch ≥12% & 200mL? Yes Asthma No COPD GOLD Staging (FEV1%) I: ≥80 | II: 50-79 III: 30-49 | IV: <30 Order DLCO Low Emphysema Nl/↑ Asthma No FVC ↓? Yes Order Lung Volumes (TLC) TLC < 80%? Yes RESTRICTIVE Order DLCO Low Interstitial Lung Disease Normal Extrapulmonary Chest wall / NM Obesity / Pleural No Normal Spirometry Suspect asthma? Methacholine Challenge Obstructive pathway Restrictive pathway Normal
09

Diagnostic Procedures

The diagnostic modalities available for assessing respiratory disease include imaging studies and techniques for acquiring biologic specimens, some of which involve direct visualization of part of the respiratory system.

Imaging Modalities

Modality Key Features Best For
Chest X-ray (PA/Lateral) Integral for parenchyma, pleura, mediastinum evaluation. Decubitus views identify free-flowing fluid. Apical lordotic views visualize lung apices better than standard PA Initial evaluation of pulmonary disease, pleural disease
Ultrasound Nonionizing radiation — safe for pregnant patients and children. Detects and localizes pleural abnormalities. Identifies septations within loculated collections. Guides percutaneous needle biopsy Pleural collections, thoracentesis guidance, peripheral lung biopsy guidance
Nuclear Medicine (V/Q Scan) Ventilation-perfusion mismatch detection using inhaled radiolabeled xenon gas. Identifies perfusion defects not accompanied by ventilation defects Pulmonary embolism evaluation
CT Cross-sectional images distinguish superimposed densities. Far better tissue density characterization and accurate lesion sizing than plain film. With IV contrast: distinguishes vascular from nonvascular structures Hilar/mediastinal disease, lung cancer staging, pulmonary embolism, pulmonary nodule characterization
Helical/MDCT Standard method for thoracic CT. Faster scans, single breath-hold acquisition, less motion artifact, thinner collimation. Data reconstructed in coronal and sagittal planes Standard thoracic CT method, continuous volumetric data acquisition
Virtual Bronchoscopy 3D reconstruction from MDCT data. Visualizes airways down to 6th–7th generation. Digital storage allows reanalysis. Assesses airway relationship to mediastinal structures Airway stenosis assessment (extent and length), pre-procedure planning for therapeutic bronchoscopy
PET Injection of 18F-FDG, taken up by metabolically active malignant cells. Detects mediastinal lymph node involvement and extrathoracic disease Solitary pulmonary nodule evaluation, lung cancer staging
MRI No ionizing radiation. Distinguishes vascular from nonvascular structures without contrast (flowing blood = no signal). Poorer spatial resolution and parenchymal detail than CT Vascular abnormalities (PE, aortic aneurysm/dissection), when CT contrast is contraindicated
Pulmonary Angiography Catheter placed in pulmonary artery, radiopaque contrast injected. Demonstrates filling defects or abrupt vessel cutoff from intravascular thrombus Pulmonary embolism diagnosis, arteriovenous malformation visualization, neoplastic PA invasion assessment
Clinical Pearl: CT reveals emphysema extent that is completely invisible on plain chest X-ray. Always consider CT when CXR findings do not match clinical severity.
Chest X-ray and CT scan from emphysema patient showing extent of disease
CXR (A) and CT (B): Emphysema extent not appreciated on plain film but clearly evident on CT
Chest X-ray and CT showing right lower lobe mass
CXR (A) and CT (B): Right lower-lobe mass. CT is superior for detecting mediastinal abnormalities
Spiral CT with sagittal reconstruction showing bronchial anastomosis
Spiral CT reconstruction in sagittal view showing anastomotic abnormality in lung transplant patient
Virtual bronchoscopic image of trachea showing carina and main stem airways
Virtual bronchoscopy: view from trachea looking down to carina with left and right main stem airways
MR angiography of lung transplant vasculature
MR angiography showing venous and arterial anastomosis after lung transplant

Specimen Collection — Medical Techniques

Sputum Collection

Spontaneous expectoration or induced (inhalation of hypertonic saline aerosol). Induction is used when sputum is not spontaneously produced or when higher yield is expected.

Quality indicators: Alveolar macrophages and inflammatory cells = lower respiratory tract origin. Squamous epithelial cells = upper airway contamination.

Sputum can be processed for: routine bacterial pathogens (Gram stain and culture), mycobacteria, fungi, viruses, and Pneumocystis jiroveci.

Percutaneous Needle Aspiration (Transthoracic)

A needle inserted through the chest wall into a pulmonary lesion to obtain aspirate or tissue core for cytologic, histologic, or microbiologic analysis. Performed under CT or US guidance for accurate needle positioning. Used for diagnosis or to decompress/drain fluid collections.

Thoracentesis

Sampling of pleural liquid performed for two purposes:

  • Diagnostic: Cellular composition and chemical constituent analysis to classify the effusion (transudate vs. exudate)
  • Palliative: Drainage of large effusion causing dyspnea

Performed by blind needle aspiration or after US localization for improved yield and safety.

Rigid Bronchoscopy

Performed in the operating room under general anesthesia. Key advantage: larger suction channel and ability to ventilate through the bronchoscope channel.

Primary indications: foreign body retrieval, massive hemorrhage suctioning (where flexible bronchoscope suction channel is insufficient).

Flexible Fiberoptic Bronchoscopy

Outpatient procedure performed under conscious sedation. Scope passed through mouth or nose, between vocal cords, into trachea. Flexible tip allows visualization to subsegmental bronchi.

Identifies: endobronchial tumors, granulomas, bronchitis, foreign bodies, bleeding sites.

Sampling methods:

  • Washing: Sterile saline instilled onto lesion surface, suctioned back for cytology and cultures
  • Brushing: Small brush at end of cable recovers cellular material for cytologic analysis
  • Biopsy: Forceps at end of cable obtains tissue for histopathologic analysis

Transbronchial Needle Aspiration (TBNA)

Hollow-bore needle passed through the bronchoscope and through the airway wall (transbronchial). Aspirates cellular material from adjacent mass lesions or enlarged lymph nodes, generally searching for malignant cells. Allows sampling without surgery or general anesthesia.

EBUS-TBNA

Ultrasonic bronchoscope fitted with a probe allowing real-time US-guided needle aspiration of mediastinal and hilar lymph nodes.

EBUS-TBNA accesses the same paratracheal and subcarinal lymph node stations as mediastinoscopy, plus extends to hilar lymph nodes (levels 10 and 11) — a key advantage over mediastinoscopy alone.

Specimen Collection — Surgical Techniques

Medical Thoracoscopy (Pleuroscopy)

Performed with a rigid or semi-rigid pleuroscope (similar in design to a bronchoscope). Allows inspection of the pleural surface, sampling and/or drainage of pleural fluid, and targeted biopsies of the parietal pleura. Focused on diagnosis of pleural-based problems.

Mediastinoscopy

Suprasternal approach under general anesthesia. Rigid mediastinoscope inserted at suprasternal notch, passed into mediastinum anterior to the trachea. Biopsy forceps sample paratracheal and pretracheal masses or nodes.

Mediastinotomy

Parasternal approach under general anesthesia. Alternative surgical route to access mediastinal masses or lymph nodes not reachable by mediastinoscopy.

Video-Assisted Thoracoscopic Surgery (VATS)

Operating room procedure using single-lung ventilation with double-lumen endotracheal intubation. Rigid scope with distal lens passed through a trocar into the pleural space. High-quality image displayed on monitor. Instruments passed through separate small intercostal incisions.

Uses: Biopsy pleural lesions under direct visualization, biopsy peripheral lung tissue, remove peripheral nodules (diagnostic and therapeutic).

Thoracotomy

Provides the largest specimen of any diagnostic sampling method. Used to biopsy or excise lesions that are too deep or too close to vital structures for VATS. Although frequently replaced by VATS, thoracotomy remains an option chosen on a case-by-case basis.

Test Your Knowledge

A sputum sample shows abundant squamous epithelial cells. What does this indicate about specimen quality, and what cell type would confirm a lower respiratory tract origin?

Squamous epithelial cells indicate upper airway contamination, meaning the sample is poor quality and does not represent lower respiratory secretions. The presence of alveolar macrophages (and other inflammatory cells) confirms a lower respiratory tract origin.

What advantage does EBUS-TBNA offer over standard mediastinoscopy for mediastinal staging?

EBUS-TBNA can access the same paratracheal and subcarinal lymph node stations as mediastinoscopy, but also extends to hilar lymph nodes (levels 10 and 11). Additionally, it uses real-time ultrasound guidance, does not require general anesthesia or a surgical incision, and provides access to more difficult-to-reach areas and smaller lymph nodes.

When would you choose rigid bronchoscopy over flexible fiberoptic bronchoscopy?

Rigid bronchoscopy is preferred for foreign body retrieval and massive hemorrhage suctioning. Its larger suction channel handles volumes of blood that overwhelm the flexible bronchoscope, and the patient can be ventilated through the rigid bronchoscope channel. It requires the operating room and general anesthesia.

10

Comprehensive Self-Assessment

22 questions covering all learning objectives. Click an answer to check yourself, then read the explanation.

1. A 58-year-old construction worker with 30 years of asbestos exposure presents for evaluation. Which of the following is NOT an accepted indication for ordering pulmonary function tests?

Correct: D. PFTs are indicated for diagnosing pulmonary disease, monitoring occupational exposures, preoperative evaluation, assessing co-morbid respiratory disease, medicolegal evaluation, and evaluating drug effects. Routine screening in asymptomatic patients without risk factors is not an indication.

2. A patient with rheumatoid arthritis develops progressive dyspnea. Her rheumatologist orders PFTs. Which indication best justifies this decision?

Correct: C. Autoimmune diseases such as rheumatoid arthritis can cause interstitial lung disease. PFTs are indicated to evaluate the severity of respiratory disease as a co-morbidity of her underlying autoimmune condition.

3. A patient with severe emphysema has PFTs showing an elevated TLC. What is the pathophysiologic explanation?

Correct: B. Emphysema causes destruction of alveolar walls, reducing the elastic recoil of the lung. With less inward recoil opposing the inspiratory muscles, the lungs expand to a larger volume, resulting in hyperinflation (elevated TLC) and air trapping (elevated RV).

4. Which of the following lung volumes CANNOT be measured by simple spirometry and requires special testing (helium dilution, nitrogen washout, or body plethysmography)?

Correct: A. Residual volume is the air remaining in the lungs after maximal forced expiration. It cannot be exhaled, so spirometry cannot measure it. RV must be estimated by helium dilution, nitrogen washout, or body plethysmography (the gold standard for lung volume measurement).

5. On a flow-volume loop, a patient demonstrates flattening of the inspiratory limb only, with a normal expiratory curve. Which condition is most consistent with this pattern?

Correct: C. Variable extrathoracic obstruction (such as vocal cord paralysis or tracheomalacia above the thoracic inlet) flattens the inspiratory limb only. During inspiration, negative intraluminal pressure causes the floppy extrathoracic airway to collapse inward. During expiration, positive pressure pushes it open, so the expiratory limb is preserved. Fixed obstruction would flatten both limbs.

6. A flow-volume loop is described as "effort-independent." What does this mean, and why is it clinically useful?

Correct: B. While spirometry values (FEV1, FVC) depend on patient effort, the shape of the flow-volume loop after peak expiratory flow is effort-independent — it reflects intrinsic airway mechanics. This means the clinician can extract diagnostic information (obstruction patterns, upper airway lesions) even when spirometric numbers might be suboptimal, and the loop shape is reproducible regardless of effort variation.

7. A 65-year-old smoker has PFTs showing FEV1 45% predicted, FVC 72% predicted, FEV1/FVC 48%, and TLC 118% predicted. Which pattern does this represent?

Correct: B. FEV1/FVC of 48% (well below 70%) defines obstruction. The elevated TLC (118%) indicates hyperinflation from air trapping, characteristic of emphysema/COPD. In restrictive disease, TLC would be reduced (<80% predicted) and the FEV1/FVC ratio would be preserved.

8. A patient with pulmonary fibrosis has PFTs performed. Which set of findings is most consistent with a restrictive pattern?

Correct: D. In restrictive lung disease, FEV1 and FVC are both reduced proportionately, so the FEV1/FVC ratio is preserved (often normal or even elevated). TLC <80% predicted confirms restriction. The hallmark: stiff, small lungs that empty proportionately, with reduced total capacity.

9. Which category of conditions causes restrictive lung disease through impairment of the inspiratory "pump" rather than intrinsic lung stiffness?

Correct: A. TLC is determined by the inspiratory pump (brain, nerves, muscles) expanding the chest wall against the lung's inward recoil. Neuromuscular disease and kyphoscoliosis restrict TLC by impairing the pump mechanism, not by making the lung itself stiffer. This distinction matters because DLCO is normal in pump failure but reduced in intrinsic lung disease.

10. What is FEV1?

Correct: C. FEV1 (Forced Expiratory Volume in 1 second) is the maximum volume of air that can be exhaled during the first second of an FVC maneuver. It is the single most important spirometric measurement for quantifying the severity of airflow obstruction.

11. A patient has FEV1 of 2.1 L (68% predicted) and FVC of 3.8 L (92% predicted). The FEV1/FVC ratio is 55%. Which statement is correct?

Correct: B. FEV1/FVC <70% defines obstruction. In this case, FEV1 is disproportionately reduced relative to FVC (FEV1 drops more than FVC in obstruction). The preserved FVC with reduced FEV1 is the classic obstructive pattern — the patient can eventually exhale the air, but flow rate in the first second is impaired.

12. A patient has normal spirometry and normal lung volumes, but a DLCO of 58% predicted. Which of the following conditions should you consider?

Correct: D. The DLCO Pearl for "isolation" (low DLCO with normal PFTs): think anemia, CHF, early interstitial lung disease, or pulmonary vascular disease. These conditions impair gas transfer at the alveolar-capillary membrane without yet producing spirometric abnormalities. Asthma has normal or high DLCO; kyphoscoliosis and obesity have normal DLCO.

13. A 62-year-old smoker has obstructive PFTs and a DLCO of 42% predicted. What is the most likely diagnosis?

Correct: A. The DLCO Pearl: low DLCO + obstruction = think emphysema. Emphysema destroys alveolar walls and capillary bed, reducing the effective surface area for gas diffusion. Asthma has normal or high DLCO despite obstruction. DLCO is a sensitive marker for the amount of lung involvement in smokers with COPD.

14. Which of the following statements about DLCO is TRUE?

Correct: C. DLCO must be ordered separately from PFTs — it is not included in a standard PFT order. It measures the ability of CO to cross the alveolar-capillary membrane from a single 10-second inhalation. Normal is 80–120% predicted; less than 80% is abnormal. The equipment is expensive and requires regular calibration, typically available at large centers.

15. Which equation correctly relates the fundamental lung volumes?

Correct: B. Total Lung Capacity equals Residual Volume plus Vital Capacity (RV + VC = TLC). VC is the difference between TLC and RV — the maximum volume that can be exhaled from full inflation. This is a fundamental relationship to memorize.

16. Functional residual capacity (FRC) is best described as:

Correct: D. FRC is the relaxation volume at the end of normal tidal expiration — the point where the elastic recoil of the lung inward equals the elastic recoil of the chest wall outward. It may be elevated in obstructive lung disease, which imposes extra load on the inspiratory muscles and can cause fatigue. Choice C describes residual volume (RV).

17. A patient with COPD has a post-bronchodilator FEV1/FVC of 62% and an FEV1 of 38% predicted. What is their GOLD stage?

Correct: C. GOLD stages are based on FEV1 % predicted (with confirmed FEV1/FVC <70%): Stage 1 = FEV1 ≥80%; Stage 2 = 50–79%; Stage 3 = 30–49%; Stage 4 = <30% (or <50% with chronic respiratory failure). FEV1 of 38% falls in the 30–49% range = Stage 3 (Severe).

18. Why should clinicians be cautious about diagnosing COPD from a single spirometry showing GOLD Stage 1?

Correct: A. GOLD Stage 1 patients frequently (up to 20%) revert to normal on repeat testing, losing the COPD diagnosis. If they stop smoking, 25% will revert to normal. This is why caution is warranted before labeling a patient with COPD based on a single borderline spirometry result.

19. A 28-year-old woman presents with episodic cough and chest tightness. Spirometry is completely normal. You strongly suspect asthma. What is the next best test?

Correct: B. When spirometry is normal but asthma is clinically suspected, a methacholine challenge (bronchoprovocation test) can demonstrate airway hyperresponsiveness. A positive test shows a significant drop in FEV1, confirming hyperreactive airways consistent with asthma. Note: methacholine challenges carry some risk and should be performed in an appropriate setting.

20. Which imaging modality is best suited for evaluating a solitary pulmonary nodule for malignancy?

Correct: D. PET scanning uses FDG uptake by metabolically active malignant cells to evaluate solitary pulmonary nodules. It helps distinguish benign from malignant nodules and is also used for lung cancer staging, including detection of mediastinal lymph node involvement and extrathoracic disease.

21. A patient presents with a large pleural effusion causing significant dyspnea. Thoracentesis is planned. What is the primary role of ultrasound in this scenario?

Correct: C. Ultrasound is nonionizing, safe, and excellent for detecting pleural abnormalities. It guides thoracentesis by localizing the fluid collection, identifying septations within loculated effusions, and improving needle placement accuracy — all of which improve yield and safety of the procedure. Fluid analysis (not imaging) determines if the effusion is malignant.

22. A 55-year-old man with suspected lung cancer requires mediastinal lymph node staging. The oncology team wants to sample paratracheal, subcarinal, AND hilar lymph nodes (levels 10–11) in a single minimally invasive procedure. Which approach is most appropriate?

Correct: A. EBUS-TBNA can access the same paratracheal and subcarinal stations as mediastinoscopy but extends to hilar lymph nodes (levels 10 and 11), which mediastinoscopy cannot reach. It uses real-time ultrasound guidance, does not require general anesthesia, and avoids a surgical incision. Mediastinoscopy (B) cannot access levels 10–11.

11

Quick Reference

Key Formulas

Obstruction
FEV1/FVC < 70% predicted
Restriction
TLC < 80% predicted
Volume Relationship
RV + VC = TLC
Abnormal DLCO
< 80% predicted (normal 80–120%)

DLCO Pearls — The Big 3

Low DLCO + Think
Obstruction Emphysema
Restriction Interstitial lung disease
Isolation (normal PFTs) Anemia, CHF, early ILD, pulmonary vascular disease
Clinical Pearl: Asthma has an obstructive pattern but DLCO is normal or high — this distinguishes it from emphysema.

GOLD Stages of COPD

Stage Severity FEV1 (% predicted)
1 Mild ≥ 80%
2 Moderate 50–79%
3 Severe 30–49%
4 Very Severe < 30% (or <50% + chronic respiratory failure)
All GOLD stages require FEV1/FVC < 70% to confirm obstruction. Caution: up to 20% of Stage 1 patients revert to normal on repeat testing.

Lung Volume Definitions

TLC
Total Lung Capacity — total volume of air in the lungs at maximal inflation
VC
Vital Capacity — difference between TLC and RV; maximum exhaled volume from full inflation
RV
Residual Volume — air remaining after maximal forced expiration (cannot be breathed out)
FRC
Functional Residual Capacity — volume remaining at end of normal tidal expiration
TV
Tidal Volume — volume of air inhaled and exhaled during normal resting breathing
FEV1
Forced Expiratory Volume in 1 sec — maximum air exhaled in the first second of FVC
FVC
Forced Vital Capacity — total air exhaled during a maximal forced expiratory maneuver

Flow-Volume Loop Patterns

Pattern Appearance
Normal Rapid rise to peak expiratory flow, nearly linear fall; symmetrical saddle-shaped inspiratory curve
Fixed Obstruction Flattened plateau on BOTH inspiratory and expiratory limbs (e.g., tracheal stenosis)
Variable Extrathoracic Flattened inspiratory limb only; normal expiratory curve (e.g., vocal cord paralysis, tracheomalacia)
Variable Intrathoracic Flattened expiratory limb only; normal inspiratory curve (e.g., intrathoracic tracheal tumor)

PFT Ordering Guide

Clinical Scenario Order
Shortness of breath Spirometry (first-line, available in most clinics)
Suspected asthma / reversible airway disease Pre- and post-bronchodilator spirometry
Normal spirometry + high clinical suspicion for asthma Methacholine challenge (bronchoprovocation)
Stridor over the neck / unexplained dyspnea Flow-volume loops
Suspected restrictive disease / diffusion impairment DLCO (must order separately from PFTs)
Need accurate lung volumes (RV, TLC) Body plethysmography (gold standard)

High-Yield Reminders

Body Plethysmography
Gold standard for measuring lung volumes (sealed chamber method)
Spirometry
Effort-dependent test — requires good patient effort and reproducibility (minimum 3 attempts)
Flow-Volume Loop
Effort-independent (after peak flow) — shape reflects airway mechanics, not effort
DLCO
Ordered SEPARATELY from PFTs — standard PFT order does NOT include DLCO
PFT Normals
Adjusted for age, gender, height, and ethnicity (ATS standards)
COPD Diagnosis
Cannot diagnose COPD without PFTs — clinical suspicion alone is insufficient
MM

Concept Mind Map

Click any node to expand or collapse it. See the complete PFT knowledge hierarchy.

Pulmonary Function Tests
Respiratory Disease Categories
Obstructive
Asthma
Reversible airflow obstruction. DLCO normal/high. Pre/post bronchodilator shows improvement.
COPD
Irreversible obstruction. FEV1/FVC < 70%. Use GOLD staging. Cannot diagnose without PFTs.
Bronchiectasis
Permanent airway dilation. Chronic cough with sputum.
Bronchiolitis
Small airway inflammation.
Restrictive
Parenchymal (Intrinsic)
ILD, pulmonary fibrosis. TLC decreased, DLCO LOW. Increased lung recoil.
Chest Wall
Kyphoscoliosis. TLC decreased, DLCO NORMAL. Pump failure.
Neuromuscular
Myasthenia gravis. TLC decreased, DLCO NORMAL. Pump failure.
Obesity
TLC decreased, DLCO NORMAL. Mechanical restriction.
Pleural
Effusion, thickening. TLC decreased, DLCO NORMAL.
Vascular
Pulmonary Embolism
V/Q mismatch. Diagnosed by CT angiography or V/Q scan.
Pulmonary Hypertension
Elevated PA pressure.
Pulmonary Veno-occlusive Disease
Rare. Post-capillary obstruction.
PFT Components
Spirometry
FEV1
Max volume exhaled in first second of FVC. Key measurement for obstruction severity.
FVC
Total volume exhaled during forced maneuver.
FEV1/FVC Ratio
< 70% = OBSTRUCTION. The defining criterion.
Effort-Dependent
Requires good patient cooperation. At least 3 reproducible attempts.
Initial Test
First PFT to order when patient presents with SOB.
Flow-Volume Loops
Axes
Volume on X-axis, Flow on Y-axis
Normal Pattern
Rapid rise to peak flow, linear fall. Saddle-shaped inspiratory curve.
Upper Airway Obstruction
Fixed (Intra or Extrathoracic)
Flattening on BOTH inspiratory AND expiratory limbs. Example: tracheal stenosis.
Variable Extrathoracic
Flattening on INSPIRATORY limb only. Examples: tracheomalacia, vocal cord paralysis.
Variable Intrathoracic
Flattening on EXPIRATORY limb only.
Obstructive Pattern
Scooped/concave expiratory curve. Reduced peak flow.
Restrictive Pattern
Similar shape to normal but SMALLER. Preserved ratio.
Lung Volumes
TLC
Total Lung Capacity. Total air in lungs. < 80% predicted = RESTRICTIVE.
FRC
Functional Residual Capacity. Air left at end of normal expiration. Elevated in obstruction.
RV
Residual Volume. Air that cannot be exhaled. Requires special testing.
VC
Vital Capacity = TLC - RV. Easily measured on spirogram.
TV
Tidal Volume. Normal resting breath volume (~500mL).
Measurement Methods
Helium Dilution
Gas dilution technique to measure communicating lung volumes.
Nitrogen Washout
Measures FRC by breathing 100% O2 and tracking N2 elimination.
Body Plethysmography
GOLD STANDARD for lung volume measurement.
Key Formula
RV + VC = TLC
DLCO
What It Measures
CO diffusion across alveolar-capillary membrane
How It Works
Single breath of CO, 10-second inhalation
Normal Range
80-120% predicted. < 80% = abnormal
Must Order Separately
NOT included in standard PFT order
The Big 3 Pearls
Low DLCO + Obstruction
EMPHYSEMA
Low DLCO + Restriction
INTERSTITIAL LUNG DISEASE
Low DLCO + Normal PFTs
Anemia, CHF, ILD, or Pulmonary Vascular Disease
Clinical Interpretation
Obstructive Pattern
Criterion
FEV1/FVC < 70%
Next Steps
Pre/post bronchodilator, DLCO
Reversible
Asthma
Irreversible
COPD → GOLD Stage
Restrictive Pattern
Criterion
TLC < 80% predicted
Next Step
Order DLCO
Low DLCO
ILD
Normal DLCO
Chest wall/NM/Obesity/Pleural
GOLD Stages of COPD
Stage 1: Very Mild
FEV1 ≥ 80%. 20% revert to normal; 25% if stop smoking.
Stage 2: Moderate
FEV1 50-80%
Stage 3: Severe
FEV1 30-50%
Stage 4: Very Severe
FEV1 < 30% or Stage 3 + low O2
Methacholine Challenge
When to Use
Normal PFT but high suspicion for asthma
What It Shows
Hypersensitive airways
Risk
Has some risk; not routine
Diagnostic Procedures
Imaging
Chest X-ray
Initial evaluation. PA + lateral views.
CT/HRCT
Superior tissue density. Lung cancer staging. Helical CT standard.
V/Q Scan
Ventilation-perfusion mismatch for PE.
PET Scan
FDG uptake in malignant cells. Pulmonary nodule evaluation.
MRI
No radiation. Good for vascular. Poor parenchymal detail.
Ultrasound
Nonionizing. Safe in pregnancy. Pleural abnormalities.
Specimen Collection
Sputum
Spontaneous or induced. Check for macrophages vs squamous cells.
Bronchoscopy
Rigid (foreign body, hemorrhage) or Flexible (standard, conscious sedation).
EBUS-TBNA
Ultrasound-guided needle aspiration. Accesses hilar nodes (levels 10-11).
Thoracentesis
Diagnostic or palliative. Pleural fluid analysis.
VATS
Video-assisted. Single-lung ventilation. Biopsy + treatment.
Thoracotomy
Largest specimens. Deep lesions.
FC

Flashcard Review

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Lung Volumes

What is TLC?

Total Lung Capacity -- the total volume of air contained in the lungs at maximum inspiration. Determined by the balance between inspiratory muscle strength and the lung/chest wall's tendency to recoil inward.

Lung Volumes

What is RV?

Residual Volume -- the volume of air remaining in the lungs after maximal forced expiration. Cannot be exhaled. Requires special testing (He dilution, N2 washout, or body plethysmography) to measure.

Lung Volumes

What is FRC?

Functional Residual Capacity -- the volume of air remaining in the lungs at the end of a normal (passive) expiration. May be elevated in obstructive disease, imposing extra load on inspiratory muscles.

Lung Volumes

What is VC?

Vital Capacity -- the difference between TLC and RV (VC = TLC - RV). The maximum volume of air that can be exhaled after a maximum inhalation.

Lung Volumes

What formula relates RV, VC, and TLC?

RV + VC = TLC. This is a fundamental relationship. If you know any two, you can calculate the third.

Lung Volumes

What does TLC < 80% predicted indicate?

Restrictive lung disease. This is the defining criterion for restriction.

Spirometry

What is FEV1?

Forced Expiratory Volume in 1 second -- the maximum volume of air exhaled during the first second of a forced vital capacity maneuver. The key measurement for obstruction severity.

Spirometry

What FEV1/FVC ratio defines obstruction?

FEV1/FVC < 70% (or < 0.70). This is the single most important number in PFT interpretation.

Spirometry

Is spirometry effort-dependent or effort-independent?

Spirometry is EFFORT-DEPENDENT. It requires a conscientious technologist and good patient effort. Results must be reproducible (minimum 3 attempts).

Spirometry

What is the initial PFT to order for a patient with dyspnea?

Spirometry. It is readily available in most clinics and assesses for airflow obstruction.

Spirometry

What are PFT results adjusted for?

Age, gender, height, and ethnicity. All results are compared to published predicted values from the American Thoracic Society.

Flow-Volume Loops

On a flow-volume loop, what is on the X and Y axes?

Volume on the X-axis, Flow (L/s) on the Y-axis. Expiratory flow is above the x-axis, inspiratory below.

Flow-Volume Loops

What does a normal flow-volume loop look like?

Expiratory: rapid rise to peak flow followed by a nearly linear fall. Inspiratory: relatively symmetrical, saddle-shaped curve.

Flow-Volume Loops

What flow-volume pattern indicates FIXED upper airway obstruction?

Flattening on BOTH the inspiratory AND expiratory limbs. Seen with tracheal stenosis (a fixed lesion present on both sides).

Flow-Volume Loops

What pattern shows VARIABLE EXTRATHORACIC obstruction?

Flattening on the INSPIRATORY limb only. During inspiration, negative pressure sucks softened trachea inward. Examples: tracheomalacia, vocal cord paralysis.

Flow-Volume Loops

What pattern shows VARIABLE INTRATHORACIC obstruction?

Flattening on the EXPIRATORY limb only. During expiration, positive intrathoracic pressure compresses the airway.

Flow-Volume Loops

Why can't standard FVC maneuvers detect upper airway obstruction?

Obstruction in the pharynx, larynx, or trachea is impossible to detect from standard FVC. Flow-volume loops are needed specifically to evaluate upper airway pathology.

Obstruction

In obstructive disease, what happens to FEV1 and FVC?

Both decrease, but FEV1 decreases MORE than FVC, causing the FEV1/FVC ratio to fall below 70%.

Obstruction

Name the major obstructive lung diseases.

Asthma (reversible), COPD (irreversible), bronchiectasis, and bronchiolitis. Obstructive diseases are MORE COMMON than restrictive.

Obstruction

What characterizes obstructive lung disease at the airflow level?

Resistance to EXPIRATORY flow. In emphysema, loss of tethering of small airways leads to collapse during expiration, increasing resistance.

Obstruction

Can you diagnose COPD without PFTs?

NO. You CANNOT diagnose COPD without PFTs. This is a critical clinical principle.

Restriction

In restrictive disease, what happens to FEV1, FVC, and their ratio?

FEV1 and FVC both decrease PROPORTIONATELY, so the FEV1/FVC ratio is PRESERVED (normal or even increased).

Restriction

What causes the decreased TLC in restrictive disease?

Either pump failure (neuromuscular disease, kyphoscoliosis) reducing chest wall expansion, OR increased inward recoil (pulmonary fibrosis) pulling lungs smaller.

Restriction

How does emphysema affect TLC?

TLC INCREASES (hyperinflation) because emphysema decreases inward recoil of the lung, allowing the lungs to over-expand and trap air.

Restriction

What is the gold standard for measuring lung volumes?

Body plethysmography -- the patient sits in a sealed chamber (like a phone booth) while pressure changes during breathing are measured.

DLCO

What does DLCO measure?

Diffusion Lung Capacity for Carbon Monoxide -- measures CO's ability to cross the alveolar-capillary membrane. Better diffusion = more CO absorbed from a single 10-second inhalation.

DLCO

What is the normal DLCO range?

80-120% of predicted. < 80% is abnormal. Some lab variation exists in upper limit.

DLCO

If DLCO is low with an OBSTRUCTIVE pattern, think...?

EMPHYSEMA. The destroyed alveolar walls reduce the surface area available for gas diffusion.

DLCO

If DLCO is low with a RESTRICTIVE pattern, think...?

INTERSTITIAL LUNG DISEASE. Fibrosis thickens the alveolar-capillary membrane, impeding diffusion.

DLCO

If DLCO is low with NORMAL PFTs (in isolation), think...?

Anemia, Congestive Heart Failure, early ILD, or Pulmonary Vascular Disease.

DLCO

What is the DLCO in asthma?

NORMAL or HIGH. This differentiates asthma from emphysema -- both are obstructive, but DLCO is preserved in asthma.

GOLD Stages

What are the GOLD stages and FEV1 cutoffs?

Stage 1 (Very Mild): ≥80% | Stage 2 (Moderate): 50-80% | Stage 3 (Severe): 30-50% | Stage 4 (Very Severe): <30% or Stage 3 + low O2

GOLD Stages

What percentage of GOLD Stage 1 patients revert to normal?

Up to 20% revert to normal. If they stop smoking, 25% revert. This is why you should be cautious about diagnosing COPD from a single spirometry.

GOLD Stages

What must be present before GOLD staging?

FEV1/FVC < 70% must be documented first to confirm COPD, THEN FEV1 alone is used for staging.

GOLD Stages

When should you order a methacholine challenge?

When PFTs are NORMAL but you highly suspect asthma. It demonstrates hypersensitive airways. Note: carries some risk.

Diagnostics

What imaging study is best for detecting mediastinal lymph node involvement?

CT with contrast, or PET scan for metabolic activity. EBUS-TBNA can sample these nodes without surgery.

Diagnostics

What does a V/Q scan detect?

Ventilation-perfusion MISMATCH -- regions with perfusion defects not accompanied by ventilation defects. Used to evaluate pulmonary embolism.

Diagnostics

What is the advantage of EBUS-TBNA over mediastinoscopy?

EBUS-TBNA accesses the same paratracheal and subcarinal nodes as mediastinoscopy PLUS hilar nodes (levels 10-11), without general anesthesia or surgery.

Clinical Pearls

DLCO must be ordered _____ from PFTs.

SEPARATELY. If you order PFTs, it will NOT include DLCO. You must explicitly order it.

Clinical Pearls

A reduced DLCO implies what?

Loss of effective capillary surface and interface. This can include thickening of the alveolar membrane (drug-induced inflammation, pulmonary edema) or destruction of alveolar walls (emphysema).