PULSE SEQUENCES · LESSON 16

Inversion recovery, STIR, and FLAIR.

Learn how timing an excitation at a tissue's zero crossing can make that tissue appear dark.

About 13 minutesRecovery-curve visual3 knowledge checks
−MzZERO+MzINVERSION TIME · TI
01EXPLAIN

START BELOW ZERO

Inversion recovery gives tissue a head start in the opposite direction.

An inversion pulse first turns longitudinal magnetization toward the negative Z direction. The tissue then begins recovering toward equilibrium. The time between that inversion pulse and the excitation pulse is called inversion time, or TI.

Different tissues recover at different rates because they have different T1 values. That means each tissue passes through zero at a different time.

IN PLAIN LANGUAGETI chooses when we look. If a tissue is at zero at that moment, it has almost no longitudinal magnetization available to tip into the transverse plane.
02VISUALIZE

CATCH THE ZERO CROSSING

Invert, wait, excite, then read the signal.

01Invert

A 180° inversion pulse turns longitudinal magnetization toward negative Z.

02Wait

The tissue recovers during the chosen TI.

03Excite

The excitation pulse is applied as the target tissue reaches zero.

04Suppress

Little longitudinal magnetization is available, so the target tissue produces little signal.

NEGATIVErecovery →0→ recoveryPOSITIVE

The exact null point is not one universal number. It depends on tissue T1, field strength, TR, sequence design, scanner, and other protocol choices.

03CONNECT

TWO IMPORTANT APPLICATIONS

STIR targets fat signal. FLAIR targets fluid signal.

STIRShort TI inversion recovery

Uses a short TI to null tissue with the short T1 of fat. It is useful when broad, reliable fat suppression is needed.

FLAIRFluid-attenuated inversion recovery

Uses a long TI to null cerebrospinal fluid while preserving T2-sensitive contrast in many brain applications.

IMPORTANT DISTINCTION

STIR is not chemically specific to fat.

STIR suppresses signal according to T1 recovery. Other short-T1 tissues, including enhancing tissue after gadolinium, may also lose signal. For that reason, STIR is generally not used to evaluate post-contrast enhancement. Always follow the approved protocol and local clinical guidance.

In the simplified case where longitudinal magnetization has fully recovered before inversion, the null point is approximately TI = 0.69 × tissue T1. Real sequences may require different timing, so scanner protocol values take priority.

04REMEMBER

THE ELEVATOR ANALOGY

Take the picture as the elevator passes the ground floor.

Imagine tissue recovery as an elevator rising from a basement floor through the lobby and upward. TI decides when the picture is taken. If the target tissue is crossing the lobby at zero when the excitation arrives, its signal is suppressed.

SSTIR

Short TI, fat signal suppressed.

FFLAIR

Fluid signal attenuated.

TIChoose the moment

Time the excitation near the target tissue's zero crossing.

Remember: Invert, wait for zero, then excite.

05APPLY

CHECK YOUR UNDERSTANDING

Match the timing to the tissue being suppressed.

What does TI measure?

TI is the time between the inversion pulse and the excitation pulse.

Which tissue signal is commonly suppressed by STIR?

STIR uses a short inversion time to suppress tissue with the short T1 of fat. It is not chemically specific to fat.

Which signal is commonly suppressed by FLAIR?

FLAIR uses a long inversion time to suppress cerebrospinal fluid, commonly while maintaining T2-sensitive image contrast.

LESSON 16 COMPLETE

You understand how inversion time can suppress selected tissue signal.

Educational references

This lesson is educational and does not replace manufacturer instructions, institutional protocols, or clinical judgment. TI values and suppression behavior vary with the scanner, field strength, sequence, and tissue.