POCUS Hub / Welcome
ED AI Tutor
Visual POCUS Curriculum

Right image · right patient · right time.

A focused, question-driven approach to bedside ultrasound. Each module opens with a complete visual guide, supplemented by interactive calculators and structured key points.

Each guide follows the same arc — indications, probe & setup, scan windows, key findings, pitfalls — so the curriculum feels familiar across modules and easy to revise.

Start here

Cognitive frameworks · scan-by-syndrome
06 STEPS
Mindset
Cognitive framework

The POCUS mindset

Six steps every scan: clinical question → probe → acquire → interpret → integrate → action. The cognitive skeleton.

Workflow
04 PROTOCOLS
Syndromes
Pattern recognition

Scan by syndrome

RUSH · CLUE · eFAST · Arrest POCUS — with pattern → diagnosis maps for the undifferentiated patient.

Resus
08 TRAPS
Pitfalls
Cognitive traps

Errors that kill scans

The cognitive shortcuts that lead to misdiagnosis — and the corrective rule for each.

Safety

Foundations atlas

Physics · knobology · artefacts
07 CONCEPTS
Physics
Wave fundamentals

The physics behind every image

Frequency, impedance, attenuation, echogenicity — why probes see what they see.

Foundations
12 CONTROLS
Knobology
Image optimisation

Dials that change diagnosis

Depth, gain, TGC, focus — the controls that turn a fuzzy scan into a diagnostic one.

Skill
11 ARTEFACTS
Atlas
Noise vs finding

Artefacts atlas

A-lines, B-lines, mirror, comet, shadow, enhancement — what's diagnostic, what to ignore.

Reference

Core foundations

View all 12 →

Integrated protocols

Advanced & specialised

Visual guide
Tap or click the image for full-size view

Ejection fraction · six methods

Cardiac · LV / RV
Method 01 · Visual Estimation

Eyeball EF

Rapid bedside qualitative read across multiple views (PLAX, PSAX, A4C). Useful for triage and trend tracking; should be confirmed with quantitative methods when image quality is adequate.

≥ 55%
Normal
Vigorous wall thickening
45–54%
Mildly reduced
Mild thickening reduction
30–44%
Moderately reduced
Visibly reduced motion
< 30%
Severely reduced
Minimal contraction
Method 02 · M-Mode

EPSS — E-Point Septal Separation

M-mode through the mitral valve in PLAX. Distance from anterior mitral leaflet (E-point) to interventricular septum at peak diastole. Larger separation correlates with poorer LV function.

EF ≈ 75.5 − (2.5 × EPSSmm) — rule of thumb only

Estimated EF ~ 58% · Normal

EPSS > 7 mm suggests reduced EF; > 13 mm strongly suggests severe dysfunction.

Method 03 · 2D Volume

Simpson's biplane

The reference-standard 2D method. Trace LV endocardial border in A4C and A2C at end-diastole and end-systole. Disk-summation calculates volumes.

EF (%) = (EDV − ESV) / EDV × 100

Ejection Fraction 60% · Normal
Method 04 · M-Mode

Teichholz & fractional shortening

From M-mode in PLAX at chordae level. Less accurate with regional wall motion abnormalities — assumes symmetric contraction.

FS = (LVIDd − LVIDs) / LVIDd × 100
Teichholz EDV = 7×LVIDd³ / (2.4 + LVIDd)

36%
Teichholz EF 63% · Normal
Method 05 · M-Mode

MAPSE — longitudinal LV

Mitral Annular Plane Systolic Excursion. M-mode at the lateral mitral annulus in A4C — measures longitudinal LV systolic motion. Independent of geometric assumptions; quick screen for LV systolic dysfunction.

Interpretation Normal · ≥ 10 mm

≥10 mm normal · 7–9 mm mild · 5–7 mm moderate · <5 mm severe dysfunction.

Method 06 · Right Ventricle

FAC — fractional area change (RV)

The RV equivalent of EF. Trace RV endocardial border in RV-focused A4C at end-diastole and end-systole. Quantifies RV systolic function.

FAC (%) = (RVEDA − RVESA) / RVEDA × 100

FAC 40% · Normal
Normal≥ 35%
Mild ↓25 – 34%
Moderate ↓15 – 24%
Severe ↓< 15%

Haemodynamics & volume status

IVC · RV pressures · congestion
Advanced · Venous Excess Ultrasound

VExUS congestion grading

Grades systemic venous congestion in cardiorenal and post-cardiac-surgery patients. Trigger is a plethoric IVC (>2 cm); then assess hepatic, portal, and intra-renal vein Doppler waveforms for severity.

VExUS Grade Grade 2 · Moderate congestion

Grade 0 = no congestion · Grade 1 = mild · Grade 2 = moderate · Grade 3 = severe (high risk of AKI). Educational reference — clinical decisions require integration with the full picture.

IVC

IVC collapsibility index

Subxiphoid IVC long-axis · M-mode 2-3 cm from RA junction. Compares max (expiration) and min (inspiration) diameters in spontaneously breathing patients.

CI (%) = (IVCmax − IVCmin) / IVCmax × 100

Collapsibility 70% · Low RAP
IVC → RAP

Right atrial pressure from IVC

ASE-recommended categorical RAP estimate from IVC max diameter and respiratory collapse — for use in RVSP calculation.

Estimated RAP 3 mmHg
Pulmonary HT

RVSP / sPAP

Right ventricular systolic pressure (≈ systolic pulmonary artery pressure in absence of RV outflow obstruction). From CW Doppler across tricuspid regurgitation jet.

RVSP ≈ 4 × (TR Vmax)² + RAP

RVSP 30 mmHg · Normal

Low < 36 mmHg · Intermediate 36–50 · Elevated > 50 mmHg.

Diastolic Function

E/e' ratio

Mitral E wave (PW Doppler at mitral valve in A4C) over septal e' wave (Tissue Doppler at medial mitral annulus). Estimates LV filling pressure when EF is preserved — useful in HFpEF assessment.

E/e' = E (cm/s) ÷ e' (cm/s)

E/e' ratio 8.9 · Normal

< 8 normal · 8 – 14 indeterminate · > 14 elevated filling pressures.

LVOT Doppler

Stroke volume & cardiac output

From LVOT diameter (PLAX, zoomed) and LVOT VTI (PW Doppler in A5C). Estimates forward flow per beat and per minute. Trends are more useful than absolute values — use serially to gauge fluid responsiveness.

CSA = π × (LVOT/2)² · SV = CSA × VTI · CO = SV × HR

63 mL
Cardiac Output 4.4 L/min

Use serially. A 12–15% rise in VTI after passive leg raise or 250 mL fluid challenge suggests fluid responsiveness.

Normal LVOT VTI in adults: ~ 18 – 22 cm.

Normal cardiac index: 2.5 – 4.0 L/min/m².

Other POCUS calculators

Vascular · Renal · Obstetric · Eye
Vascular

AAA classifier

Outer-wall to outer-wall AP diameter in transverse view at largest diameter.

Classification Normal · < 3 cm
Renal

Bladder volume

Three orthogonal bladder dimensions on suprapubic ultrasound.

V (mL) ≈ L × W × H × 0.52

Volume 175 mL
Obstetric

CRL → gestational age

Crown-Rump Length is the most accurate dating measurement at 6–13⁺⁶ weeks.

GA (weeks) ≈ (CRLmm + 42) / 7

Gestational Age 8w 1d

Cardiac activity expected at CRL ≥ 7 mm. FHR normal 110–160 bpm at 6–7 weeks.

Ocular · ICP

Optic nerve sheath diameter

Linear high-frequency probe, transverse axial view, 3 mm posterior to retina, outer-to-outer measurement. NO pressure on the globe.

Interpretation Normal · ≤ 5 mm

Adults: ≤5 normal · 5.1–5.5 borderline · >5.5 suggests raised ICP · >6.0 high suspicion. Paeds use age-adjusted (≈ ≤ 4.5–5 mm).

Renal · Reference

Hydronephrosis grading (SFU)

Society for Fetal Urology system — qualitative grading of pelvicalyceal dilatation on bedside renal ultrasound.

0
None
Central echo complex intact · no dilatation
1
Mild
Pelviectasis only · renal pelvis dilated
2
Mild–Mod
Pelvis + a few major calyces dilated
3
Moderate
Pelvis + major & minor calyces dilated
4
Severe
Marked dilatation · cortical thinning

Clinical question

Define what you must know right now to act. Without this, every other step is wasted. The probe is a tool to answer a question, not a fishing expedition.

"What finding would change my next action?"

Best probe & view

Match probe and window to the question. Cardiac → phased array. Trauma → curvilinear. Vessels and procedures → linear. Don't choose by habit; choose by the question.

"What probe + view answers this fastest?"

Acquire image

Optimise depth, gain, focus. Use orthogonal planes. Save clips, not just stills. If you can't get the view, document inadequate windows — don't pretend.

"Is this image diagnostic, or am I guessing?"

Interpret findings

Compare to normal. Look for both positives and negatives. Beware confirmation bias. The eye sees what the brain expects unless you actively disagree with yourself.

"What argues against my leading hypothesis?"

Integrate

POCUS finding plus history, vitals, labs, ECG, prior imaging. POCUS never travels alone. A finding is only as useful as its place in the bigger picture.

"Does the picture as a whole make sense?"

Action & document

Communicate the safe, informed decision. Document the scan, findings, limitations, and the action they drove. Close the loop with the team.

"Have I closed the loop with the team?"
Rapid Ultrasound for Shock & Hypotension

Five-domain sweep · HIMAP

Mnemonic: HI MAP — when the patient is low MAP, restore them to HI MAP. Heart, IVC, Morrison's, Aorta, Pulmonary.

H
Heart
EF · RV strain · pericardial effusion · regional wall motion
I
IVC
Collapsible → hypovolaemic / distributive · plethoric → obstructive / cardiogenic
M
Morrison's
Haemoperitoneum · haemothorax · trauma sweep
A
Aorta
AAA · aortic dissection (intimal flap, lumen diameter)
P
Pulmonary
Pneumothorax · B-lines · effusion
Pattern
Likely diagnosis
Reduced EF + diffuse B-lines
Cardiogenic / acute pulmonary oedema
Hyperdynamic LV + flat IVC
Distributive / hypovolaemic
Dilated RV + small LV + clear lungs
Massive PE / obstructive shock
Pericardial effusion + plethoric IVC + chamber collapse
Tamponade
Free abdominal fluid + shock
Haemorrhage until proven otherwise
AAA > 3 cm + shock
Ruptured AAA — resus → OT
Aortic intimal flap
Aortic dissection — BP control + CT
Cardiac & Lung Ultrasound Exam

Combined echo + lung profile

Rapid combined echo and lung ultrasound for acute dyspnoea, chest pain with breathlessness, peri-arrest physiology. Designed to distinguish CHF, COPD/asthma, pneumonia, PE pattern, and tamponade.

01
PLAX
LV function · pericardial effusion · aortic root
02
A4C
RV:LV ratio · gross valves · chamber size
03
Sub-x + IVC
Pericardium · venous pressure proxy
04
Lung zones
Sliding · A-lines · B-lines · effusion
Pattern
Likely diagnosis
Bilateral B-lines + poor LV
Cardiogenic pulmonary oedema
Bilateral B-lines + preserved LV + sepsis
ARDS / pneumonia / non-cardiogenic
A-lines + wheeze + normal LV
Asthma / COPD more likely
Unilateral absent sliding + lung point
Pneumothorax
RV:LV > 1 + D-shaped septum + clear lungs
PE concern · integrate ECG / CTPA
Extended Focused Assessment with Sonography in Trauma

The trauma five

Answers four questions in under three minutes: free fluid in abdomen / pelvis / pericardium, and pneumothorax. Negative does not exclude — sensitivity is reduced for retroperitoneal and small-volume bleeds. Repeat when the patient changes.

1
RUQ
Morrison's pouch + lung base
2
LUQ
Splenorenal + lung base
3
Pelvis
Pouch of Douglas / retro-vesical
4
Sub-x
Pericardial effusion
5
Lungs
Bilateral anterior — pneumothorax
Finding + status
Action
Positive eFAST + unstable
Trauma team · operative path
Positive eFAST + stable
CT trauma per pathway · monitor
Negative eFAST + unstable
Look elsewhere — chest, retroperitoneum, sepsis, neurogenic
Pericardial effusion
Possible tamponade · senior + pericardiocentesis prep
Absent sliding + lung point
Pneumothorax · needle / chest drain
Cardiac Arrest POCUS

Reversible cause sweep

Used during the rhythm check pause (≤10 seconds) to identify reversible causes. Performed by a dedicated team member; must not delay compressions or rhythm-check timing. Subxiphoid is the workhorse view; lung is the backup.

01
Sub-x heart
Effusion · contractility · chamber size
02
IVC
Plethoric or flat — preload clue
03
Lungs
Bilateral sliding — exclude tension
04
DVT (if time)
Femoral / popliteal — PE clue
Finding
Reversible cause
Pericardial effusion + chamber collapse
Tamponade — pericardiocentesis
Absent lung sliding + lung point
Tension pneumothorax — decompress
Dilated RV + flat LV ± DVT
Massive PE — consider thrombolysis
Hyperdynamic empty LV + flat IVC
Hypovolaemia / haemorrhage — fluids / blood
Cardiac standstill on pause
Poor prognosis — discuss termination of efforts
View Window / target eFAST FELS RUSH CLUE Arrest Focused app
SUB-XSubxiphoid 4-chamberEcho
PLAXParasternal long axisEcho
PSAXParasternal short axisEcho
A4CApical 4-chamberEcho · TAPSE · EF
IVCSubxiphoid IVC longEcho · VExUS
RUQHepatorenal · Morrison'seFAST · Renal · GB
LUQSplenorenaleFAST · Renal
PELVISSuprapubic / Pouch of DouglaseFAST · OB · Renal
AORTATrans + long axisAAA
LUNG-ANTBilateral anterior chestLung
LUNG-LATLateral / base · effusionLung
CFV / POPCompression DVT scanDVT
OCULARTrans + sag · ONSDOcular · raised ICP
TVUSEndocavityOB · Gyn · early pregnancy
Core view — protocol fails without it
Adjunct — adds discriminating information
Not part of this protocol
i
"I saw no free fluid, so there's no bleeding."
FixFAST can be falsely negative early or in retroperitoneal bleeds. Repeat the scan. CT if stable. Escalate if not.
ii
"IVC is flat — give lots of fluid."
FixIVC is affected by ventilation, RV failure, intrathoracic pressure, and patient effort. Use lungs, LV, RV, and a dynamic perfusion response together — never IVC alone.
iii
"RV dilated = PE."
FixChronic pulmonary HT, RV infarct, and ARDS all cause RV strain. Integrate history, ECG, DVT scan, and the CTPA pathway. Never call PE from RV findings alone.
iv
"No lung sliding = pneumothorax."
FixMainstem intubation, pleurodesis, apnoea, and pleural adhesions all abolish sliding. Confirm with the lung point — the only highly specific sign.
v
"Thick gallbladder wall means cholecystitis."
FixCHF, hepatitis, and hypoalbuminaemia all thicken the wall. Need stones + sonographic Murphy's + clinical context to call acute cholecystitis.
vi
"POCUS replaces CT or formal echo."
FixPOCUS is focused and operator-dependent. It answers immediate bedside questions. Formal imaging follows when indicated — they are complementary, not substitutes.
vii
"Foreshortened A4C — looks like RV is dilated."
FixAnchor on the apex first. A foreshortened apex artificially compresses LV and exaggerates RV size. Re-acquire the full chamber length before calling RV strain.
viii
"Anterior fat pad must be a pericardial effusion."
FixTrue effusion tracks circumferentially. Epicardial fat is anterior and bright on the same side. Confirm with a second view (sub-x or apical) before calling effusion.
i

Phase 01 · Foundations

Master probe handling, orientation, knobology, image optimisation, normal anatomy, documentation, and infection control. Build the muscle memory before adding complexity.

Lung scans25
Cardiac views25
eFAST exams25
AAA scans15
Renal / bladder15
Vascular access15
ii

Phase 02 · Syndrome-based scanning

Every resus patient gets a structured POCUS workflow: clinical question → three views → finding that changes management → backup plan. Move from "what does it look like?" to "what does it mean?"

RUSH scans20
CLUE scans20
Arrest / peri-arrest10
Trauma eFAST10
DVT scans10
Biliary scans10
iii

Phase 03 · Advanced integration

VTI, venous congestion, tamponade physiology, lung profiles, procedural needle guidance, serial reassessment. POCUS as part of a continuous resus loop — not a one-shot snapshot.

LV gradingAdvanced
RV strain patternsAdvanced
VTI / stroke volAdvanced
VExUS scoringAdvanced
Nerve blocksAdvanced
PericardiocentesisAdvanced
01 · Wave properties

Frequency & wavelength

Ultrasound is sound above 20 kHz; diagnostic POCUS uses 2–20 MHz. Higher frequency means shorter wavelength, which gives finer detail but penetrates less. Wavelength = speed of sound ÷ frequency.

λ = c ÷ f  ·  ctissue ≈ 1540 m/s
ClinicalHigher MHz → superficial detail (vessels, MSK). Lower MHz → deep penetration (heart, abdomen).
02 · The trade-off

Probe frequency vs depth

You cannot have both. Choose probe by depth of target, not familiarity. Linear (7–15 MHz) for superficial structures. Curvilinear (2–5 MHz) for abdomen/lung. Phased array (1–5 MHz) for heart through narrow rib spaces.

Linear7–15 MHz · 0–6 cm · vessels, MSK, lung, eyes, procedures
Curvilinear2–5 MHz · 4–25 cm · abdomen, AAA, OB, lung, eFAST
Phased1–5 MHz · cardiac · small footprint between ribs
Endocavity5–9 MHz · TVUS · early pregnancy, pelvis
03 · Tissue interaction

Acoustic impedance

Resistance a tissue offers to sound transmission. Z = density × velocity. At any interface where impedance changes, some sound reflects (becomes the image) and some transmits. Big mismatches (air ↔ tissue, bone ↔ tissue) reflect almost everything — which is why air and bone appear bright with shadow behind, and why gel matters.

Z = ρ × c  ·  air ≈ 0.0004, soft tissue ≈ 1.6, bone ≈ 7.8 (×10⁶ rayl)
PearlCouple to skin with gel — air pocket = ~99% reflection = no image.
04 · Energy loss

Attenuation

As the wave travels deeper, energy is lost to absorption (heat), reflection, and scattering. Attenuation increases with depth and with frequency — another reason high-frequency probes can't see deep. Time Gain Compensation (TGC) on the machine compensates for this fade.

ImplicationBone strongly attenuates → distal shadow. Fluid weakly attenuates → distal enhancement.
05 · The vocabulary

Echogenicity scale

How bright a structure appears on ultrasound, relative to its surroundings. The vocabulary every report uses:

Anechoic
Pure fluid: bladder, blood, simple cyst
Hypoechoic
Solid organs, muscle, complex fluid
Isoechoic
Same brightness as a reference tissue
Hyperechoic
Fascia, fat, tendons, calcifications
Echogenic shadow
Bone surface, gallstones — bright + shadow behind
06 · Image quality

Axial vs lateral resolution

Axial resolution (along the beam) is the ability to separate two structures stacked along the beam path; it depends on wavelength and is always the better of the two. Lateral resolution (across the beam) depends on beam width and is best at the focal zone — which is why you adjust focus to the level of interest.

PearlIf something looks fuzzy laterally, drop the focus marker to that depth.
07 · The constant

Speed of sound

The machine assumes 1540 m/s in soft tissue to calculate depth from echo return time. When the wave passes through tissue with a different speed (fat ~1450, bone ~4080) the geometry assumption breaks — and that's where many artefacts come from.

depth = (speed × time) ÷ 2
01
Patient
02
Probe + preset
03
Depth
04
Gain + TGC
05
Focus
06
Freeze · save
01 · DEPTH
How deep to look

Set so the structure of interest fills the lower two-thirds of the screen. Too shallow → cropped target. Too deep → tiny target, wasted resolution.

"Target in the lower two-thirds."
02 · GAIN
Overall brightness

Amplifies returning echoes. Set so blood/fluid is black and tissue planes have full grey-scale range. Over-gained = washed out, under-gained = misses subtle pathology.

"Black should look black."
03 · TGC
Time gain compensation

Sliders that adjust gain at specific depths to compensate for attenuation. Top sliders = near field, bottom sliders = far field. Aim for uniform brightness top to bottom.

"Even brightness at every depth."
04 · FOCUS
Focal zone placement

Concentrates the beam at a chosen depth, sharpening lateral resolution at that level. Place the focus marker at the depth of interest — usually mid-image.

"Focus where it matters."
05 · FREQUENCY
Within probe range

Many probes have a frequency toggle (low / mid / high). Higher frequency = better resolution, less penetration. Drop to lower frequency in larger patients or when imaging deep structures.

"Highest MHz that still penetrates."
06 · HARMONICS
Tissue harmonic imaging

Uses the second harmonic frequency from tissue to reduce noise and improve contrast in difficult bodies. Often labelled "THI" — turn on for adult abdominal and cardiac scans.

"On for the difficult belly."
07 · DYNAMIC RANGE
Greyscale contrast

Range of echo intensities displayed. Wide range = soft, smooth image (cardiac). Narrow range = high contrast (procedures, MSK). Most presets handle this — touch only if needed.

"Soft for hearts, sharp for needles."
08 · ZOOM
Magnify a region

Two flavours: read zoom (magnifies pixels — no extra detail) and write zoom (re-acquires data, true higher resolution). Always prefer write zoom when measuring (e.g. AAA diameter).

"Write zoom for measurements."
09 · FREEZE · CINE · SAVE
Capturing the image

Freeze captures the live image. Cine scrolls back through the previous seconds — invaluable for grabbing the systolic frame or a B-line. Save clips, not just stills, for cardiac and lung.

"Save clips for cardiac and lung."
10 · PRESETS
Pre-tuned settings

The machine's starting point: cardiac, abdominal, OB, MSK, vascular. Each adjusts dynamic range, harmonics, frame rate, and orientation. Always start from the right preset before fiddling.

"Right preset first; tweak second."
11 · INDICATOR
Probe orientation marker

The notch / dot on the probe corresponds to a marker on the screen. Convention: cardiology has indicator on screen-right, all other applications screen-left. Check before every scan.

"Cardiac right · everything else left."
12 · MODE BUTTONS
B-mode · M-mode · Doppler

B-mode is the 2D greyscale default. M-mode shows one line over time (TAPSE, lung sliding). Colour Doppler shows flow direction. PW/CW Doppler quantifies velocities at a point or peak.

"Master B-mode before adding Doppler."
PLEURAL LINE
A-lines · reverberation off pleura
Finding · normal lung
MechanismSound bounces between probe and the pleural line at regular intervals — the machine paints each return as if it were a deeper structure, producing equally-spaced horizontal lines.
RecognitionBright pleural line + parallel horizontal echoes at multiples of the probe-to-pleura distance.
MeansAerated lung. With sliding present → rules out pneumothorax at that intercostal space.
PLEURAL LINE
B-lines · vertical comet artefact
Finding · interstitial syndrome
MechanismReverberation between thickened, fluid-filled interlobular septa — produces a vertical hyperechoic line that extends to the bottom of the screen, moves with sliding, and erases A-lines.
Recognition≥ 3 B-lines per intercostal field is pathologic. Bilateral diffuse → cardiogenic pulmonary oedema. Patchy / unilateral → ARDS, pneumonia, contusion.
MimicZ-lines are short and don't reach the bottom — ignore.
Reverberation
Context-dependent
MechanismSound trapped between two strongly reflective parallel surfaces (pleura ↔ probe, metal needle, prosthetic valve) bounces back and forth, producing equally-spaced parallel echoes that fade with depth.
RecognitionMultiple parallel lines at equal spacing, decreasing intensity.
ExamplesA-lines (lung — finding), needle shaft on a procedure scan (finding — helps identify the needle), bowel gas reverb (noise).
Comet tail · close-spaced reverb
Finding · marker
MechanismReverberation between two reflectors that are very close together (sub-millimetre) — individual reflections blur into a tapering bright tail.
RecognitionShort, triangular, fades with depth.
ExamplesNeedle tip on a procedure scan (helpful — confirms the tip), gallbladder wall adenomyomatosis ("comet tail in the wall" — Rokitansky-Aschoff sinuses with cholesterol).
Ring down
Context-dependent
MechanismAir bubble resonates when struck by the beam, emitting a continuous sound wave back to the probe — paints as a long, thin, persistent hyperechoic streak that does not fade with depth.
RecognitionLong bright line behind a tiny bright source, full screen depth, sharp edges.
ExamplesBowel gas (noise), pneumobilia (finding — air in biliary tree), abscess gas.
DIAPHRAGM
Mirror image
Noise · don't be fooled
MechanismA strong curved reflector (most often the diaphragm) bounces sound off a real structure and back, so the machine paints a copy of that structure on the far side of the reflector.
Recognition"Liver above the diaphragm" — that's the mirror, not real lung pathology. Equal distance from the reflector.
PitfallCalling a mirrored liver/spleen above the diaphragm "consolidated lung" on FAST or BLUE.
Acoustic shadowing
Finding · diagnostic
MechanismA strongly attenuating structure (bone, gallstone, calcified plaque) absorbs / reflects the beam — almost no sound reaches deeper, so the area distal to it is black.
RecognitionSharp dark band directly behind a bright structure.
MeansGallstone with shadow + sonographic Murphy's = high-yield for cholecystitis. Renal stone, bone (rib), calcified atheroma.
Edge shadow
Noise · refraction
MechanismAt the curved edge of a fluid-filled structure (gallbladder, bladder, cyst, large vessel), the beam refracts away — creating thin shadows extending from the lateral edges of the structure.
RecognitionTwo narrow dark stripes radiating from the lateral margins of a round anechoic structure.
PitfallConfusing edge shadow with a stone — stones cast shadow from inside the lumen, edge shadows come from the lateral margin.
Acoustic enhancement
Finding · indicator
MechanismFluid attenuates sound less than tissue, so the beam reaches the structure behind a fluid-filled area at higher intensity than the surrounding TGC accounts for — the area distal looks abnormally bright.
RecognitionBright band directly deep to an anechoic structure.
Useful forConfirming a cyst is truly fluid-filled. Spotting pleural effusions ("spine sign" — vertebral bodies become visible deep to fluid).
Side lobe
Noise · false echo
MechanismA small fraction of beam energy travels off the central axis. If it hits a strong reflector off-axis, the machine still paints the echo as if it came from the central axis — creating false structures inside fluid-filled cavities.
RecognitionCurved or hazy debris inside the bladder or gallbladder that disappears on a slightly different angle.
PitfallCalling side-lobe debris in the bladder "stones" or "sediment". Reposition and re-scan; real material persists.
LUNG POINT
Lung point
Finding · pathognomonic
MechanismThe interface where pneumothorax meets normal pleura — the visualised transition between absent sliding/A-lines (PTX) and normal sliding (aerated lung) on B-mode or as a "barcode → seashore" transition on M-mode.
RecognitionClear single-frame transition; on M-mode, a vertical shift between two patterns at the same intercostal level.
MeansHighly specific for pneumothorax — confirms when seen, but absence does not exclude (a complete pneumothorax has no lung point).