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Published on: July 18, 2016
Central post stroke pain: clinical, MRI, and SPECT correlation
Jayantee Kalita1, Bishwanath Kumar, Usha K Misra
1Department of Neurology, Sanjay Gandhi PGIMS, Lucknow, India. jayanteek@yahoo.com
Pain Medicine (Malden, Mass.)
|January 27, 2011
Summary
Central post-stroke pain (CPSP) showed similar quantitative sensory testing (QST) findings regardless of lesion location. Magnetic resonance imaging (MRI) and single photon emission computed tomography (SPECT) results did not differ between patients with or without allodynia.
Area of Science:
- Neurology
- Neuroimaging
- Pain Medicine
Background:
- Central post-stroke pain (CPSP) is a debilitating neurological condition resulting from stroke-induced damage to the somatosensory pathways.
- Understanding the clinical spectrum and neuroimaging correlates of CPSP is crucial for effective diagnosis and management.
- Quantitative sensory testing (QST) provides objective measures of sensory dysfunction in pain conditions.
Purpose of the Study:
- To characterize the clinical presentation of central post-stroke pain (CPSP).
- To correlate clinical findings with magnetic resonance imaging (MRI) and single photon emission computed tomography (SPECT) in CPSP patients.
- To investigate the relationship between QST findings and neuroimaging results in CPSP.
Main Methods:
- A prospective study involving 23 consecutive patients with CPSP was conducted at a tertiary care teaching hospital.
- Quantitative sensory testing (QST) assessed pain severity, sensory thresholds, allodynia, hyperalgesia, and temporal summation.
- Cranial MRI and technetium-99m ethylene cystine dimmer SPECT were performed and correlated with QST findings.
Main Results:
- QST findings were comparable between patients with thalamic and extrathalamic CPSP lesions.
- MRI revealed infarction in 14 patients and hematoma in nine patients.
- SPECT showed abnormalities in 17 patients, with hypoperfusion in the thalamus (n=9) and parietal cortex (n=11); however, MRI and SPECT findings did not differ in patients with or without allodynia.
Conclusions:
- Clinical and QST characteristics of CPSP are similar irrespective of whether the lesion is located in the thalamus or extrathalamic regions.
- Neuroimaging findings (MRI and SPECT) do not differentiate CPSP patients based on the presence or absence of allodynia.
- Further research is needed to elucidate the complex mechanisms underlying CPSP and identify specific imaging biomarkers.
