Evaluation of MR perfusion abnormalities in organophosphorus poisoning and its correlation with SPECT.

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Evaluation of MR perfusion abnormalities in organophosphorus poisoning and its correlation with SPECT.

Indian J Radiol Imaging. 2017 Jan-Mar;27(1):36-42

Authors: Bhanu KU, Khandelwal N, Vyas S, Singh P, Prabhakar A, Mittal BR, Bhalla A

Abstract
AIM: Acute organophosphate (OP) pesticide poisoning causes substantial morbidity and mortality worldwide. Many imaging modalities, such as computerized tomography (CT), magnetic resonance imaging (MRI), and single photon emission computed tomography (SPECT) of the brain, have been used for quantitative assessment of the acute brain insult caused by acute OP poisoning. Perfusion defects on SPECT in acutely poisoned patients with OPs have been described, however, MR perfusion abnormalities have not been described in the literature. MR perfusion Imaging has the advantage of having higher spatial resolution, no radiation, and better availability.
MATERIALS AND METHODS: In this prospective study, 20 patients who ingested OP compounds were included. All the patients underwent brain SPECT on a dual head SPECT gamma camera and MRI brain on a 1.5T MR system. Neurocognitive tests were performed for all patients.
RESULTS: SPECT showed perfusion defects in 7 patients and total number of perfusion defects were 29. On MR perfusion, based on the cut-off values of normalized cerebral blood volume (nCBV) ratios and normalized cerebral blood flow (nCBF) ratios, the total number of patients showing perfusion defects were 6 and 8; and the total number of perfusion defects were 29 and 45, respectively. There was significant difference of the nCBV ratios and nCBF ratios between the control group (n = 20) and positive patients group (n = 6 and n = 8, respectively) (P > 0.05). All the defects seen on SPECT were well appreciated on nCBF maps (MRI perfusion) suggestive of 100% correlation.
CONCLUSION: MR perfusion imaging can be used as an effective modality for evaluation in acute OP poisoning.

PMID: 28515582 [PubMed - in process]

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