SPECT Brain Imaging
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Brain perfusion single-photon emission computed tomography (SPECT) imaging is a functional nuclear imaging technique performed to evaluate regional cerebral perfusion.
Because cerebral blood flow is closely linked to neuronal activity, the activity distribution is presumed to reflect neuronal activity levels in different areas of the brain. A lipophilic, PH-neutral radiopharmaceutical (most commonly99m Tc-hexamethylpropyleneamine oxime [HMPAO] and99m Tc-ethylene cysteine diethylester [ECD], with a half-life of 6.02 hours) is injected into the patient, which crosses the blood-brain barrier and continues to emit gamma rays. [1, 2] A 3-dimensional representation of cerebral blood flow can be iterated using gamma detectors, allowing for interpretation.
Brain SPECT can be complemented with pharmaceutical agents that enhance regional cerebral blood flow, such as acetazolamide (carbonic anhydrase). Acetazolamide increases local pCO2 and causes arteriolar dilation, allowing for assessment of cerebrovascular reserve in transient ischemic attack, stroke, and vascular anomalies and distinguishing vascular from neuronal causes of dementia. [3]
Brain SPECT imaging has many different clinical applications.
Brain perfusion SPECT imaging can aid in the diagnosis and ongoing evaluation of many different medical conditions, as follows:
Detection and evaluation of cerebrovascular disease
Aid in the diagnosis and differential diagnoses of suspected dementia
Detection of seizure focus
Assessment of brain death
Evaluating suspected brain trauma
Neuropsychiatric disorders: Mood disorders, evaluating and subtyping attention-deficit disorder
Substance abuse
Infection/inflammation
Brain SPECT imaging is contraindicated in the following:
Pregnancy
Breastfeeding (this should be interrupted for 24 hours prior to imaging)
Lack of cooperation
Brain SPECT imaging is a safe procedure on the whole. However, care must be provided by the imaging technologist to reduce patient discomfort and minimize motion artifact. Care must also be provided to avoid tissue extravasation of radiopharmaceutical agents, as there is potential to induce tissue necrosis.
Juni JE, Waxman AD, Devous MD Sr, Tikofsky RS, Ichise M, Van Heertum RL, et al. Procedure guideline for brain perfusion SPECT using (99m)Tc radiopharmaceuticals 3.0. J Nucl Med Technol. 2009 Sep. 37(3):191-5. [Medline].
Kapucu OL, Nobili F, Varrone A, Booij J, Vander Borght T, Någren K, et al. EANM procedure guideline for brain perfusion SPECT using 99mTc-labelled radiopharmaceuticals, version 2. Eur J Nucl Med Mol Imaging. 2009 Dec. 36(12):2093-102. [Medline].
Farid K, Petras S, Ducasse V, Chokron S, Helft G, Blacher J, et al. Brain perfusion SPECT imaging and acetazolamide challenge in vascular cognitive impairment. Nucl Med Commun. 2012 Jun. 33(6):571-80. [Medline].
Kranert T, Menzel C, Bartenstein P, Brust P, Coenen HH, Krause BJ, et al. [Perfusion brain imaging with SPECT-technique. German Guideline S1]. Nuklearmedizin. 2013. 52(5):157-62; quiz N55. [Medline].
Thrall J, Ziessman H. Central Nervous System. Nuclear Medicine – The Requisites. 1st Ed. United States of America: Mosby; 1995. Nuclear Medicine: 11.
Murray I.P.C, Ell P.J. Lipophilic tracers for the study of regional cerebral blood flow. Van der Wall.H, William Strauss.H. Nuclear Medicine in Clinical Diagnosis and Treatment. 2nd Ed. Edinburgh: Churchill Livingstone; 1998. 1: 42.
Tc99m-HMPAO (Ceretec®)
Tc99m-ECD (Neurolite®)
Transport mechanism
Neutral lipophilic compound
Neutral lipophilic compound
First First-pass cerebral extraction
80%
60%-70%
Peak activity
1-2 minutes postinjection
4%-7% of the dose remains within the brain
1-2 minutes postinjection
6%-7% of the dose remains within the brain
Advantage
Less radiation dose
Rapid brain uptake with excellent brain retention
Higher brain-to-background ratio
Higher gray-to-white matter ratio
Disadvantage
Poor stability
Dose needs to be used within 30 minutes postreconstitution
Higher radiation dose
Currently not available in Australia
Trapping mechanism
Trapped in all living cells; glutathione-mediate conversion to hydrophilic complex
Trapped only in metabolically intact cells and not retained during transient dysfunction; enzymatic (esterases) conversion to hydrophilic products
Radiopharmaceutical
Administered Activity, MBq (mCi)
Organ Receiving the Largest Radiation Dose, mGy (rad)
Effective Dose, mSv (rem)
Tc-99m HMPAO
555-1110 IV
(15-30)
0.034
Kidneys
(0.126)
0.0093
(0.034)
Tc-99m ECD
555-1110 IV
(15-30)
0.073
Bladder wall
(0.27)
0.011
(0.041)
Radiopharmaceutical
Administered Activity,
MBq/kg
(mCi/kg)
Organ Receiving the Largest Radiation Dose, mGy (rad)
Effective Dose, mSv (rem)
Tc-99m HMPAO
7.4–11.1 IV
(0.2-0.3)
0.14
Thyroid
(0.52)
0.026
(0.096)
Tc-99m ECD
7.4-11.1 IV
(0.2-0.3)
0.083
Bladder wall
(0.31)
0.023
(0.085)
Matthew Tam, MBBCh Resident Physician, Nuclear Medicine, Royal Perth Hospital, Australia
Disclosure: Nothing to disclose.
Sylvia Suk Kwan Leung, MPH Nuclear Medicine Technologist, Certified Densitometry Technologist, Department of Nuclear Medicine, Royal Perth Hospital, Australia
Disclosure: Nothing to disclose.
Michael McCarthy, MBBS, FRACP, ANZAPNM Head of Department, Nuclear Medicine Specialist, Department of Nuclear Medicine, Royal Perth Hospital; Nuclear Medicine Imaging Specialist, Perth Radiology Clinics, Australia
Disclosure: Nothing to disclose.
Gowthaman Gunabushanam, MD, FRCR Assistant Professor, Department of Diagnostic Radiology, Yale University School of Medicine
Gowthaman Gunabushanam, MD, FRCR is a member of the following medical societies: American Roentgen Ray Society, Connecticut State Medical Society
Disclosure: Nothing to disclose.
SPECT Brain Imaging
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