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Brain involvement in organophosphate poisoning

dc.contributor.buuauthorYılmazlar, Aysun
dc.contributor.buuauthorÖzyurt, Gürayten
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentAnesteziyoloji ve Yoğun Bakım Ana Bilim Dalı
dc.date.accessioned2021-08-31T06:44:08Z
dc.date.available2021-08-31T06:44:08Z
dc.date.issued1997
dc.description.abstractOrganophosphate poisonings cause substantial morbidity and mortality worldwide; however, the neurological effects have not been clearly established. We have studied cerebral perfusion to investigate neurotoxic effects. Clinical effects, plasma cholinesterase activity, and brain single photon emission computerization tomography (SPECT) data were investigated in 16 patients with organophosphate poisonings. The subjects were from an adult intensive care unit in a university hospital. Cholinesterase activity in plasma was determined upon admission and then every day in the morning. Brain SPECT studies were performed during the first seek, at the end of therapy, and 3 months after discharge. Patients were classified into 3 groups using a modified Namba classification: latent poisoning (Group A); mild and moderate poisoning (Group B); or severe poisoning (Group C). None of the 6 patients in Group A showed any symptoms; 3 patients in Group B had muscarinic and nicotinic effects; 5 patients in Group C had muscarinic, nicotinic, and central nervous system symptoms. The average plasma cholinesterase for Groups A, B, and C were 54.16 +/- 9.10, 42.2 +/- 12.02, and 13 +/- 4.84 U/ml, respectively (normal range of plasma cholinesterase is 40-80 U/ml). Only 1 patient from Group A required treatment with oxime; 2 patients from Group B and all patients in Group C were given oxime, atropine sulfate, and mechanical ventilation. In the brain SPECT studies, the patients in Group A showed fewer perfusion defect areas than did Group B and C patients. All cases showed perfusion defects especially in the parietal lobe. In addition, perfusion improvement took more time for Group C than for the other groups. The intensive care unit stays of Group C were statistically longer than for Groups A and B. We concluded that brain SPECT is a highly sensitive diagnostic method, together with clinical symptoms and plasma cholinesterase activity, for monitoring the clinical prognosis of organophosphate poisonings.
dc.identifier.citationYılmazlar, A. ve Özyurt, G. (1997). "Brain involvement in organophosphate poisoning". Environmental Research, 74(2), 104-109.
dc.identifier.doi10.1006/enrs.1997.3758
dc.identifier.endpage109
dc.identifier.issn0013-9351
dc.identifier.issue2
dc.identifier.pubmed9339222
dc.identifier.scopus2-s2.0-0031214468
dc.identifier.startpage104
dc.identifier.urihttps://doi.org/10.1006/enrs.1997.3758
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0013935197937580
dc.identifier.urihttp://hdl.handle.net/11452/21563
dc.identifier.volume74
dc.identifier.wosA1997YC68600002
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherAcademic Press Inc Elsevier Science
dc.relation.journalEnvironmental Research
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectEnvironmental sciences & ecology
dc.subjectPublic, environmental & occupational health
dc.subjectBlood-flow
dc.subjectIntoxication
dc.subjectNeurotoxicity
dc.subjectNeuropathy
dc.subjectMetabolism
dc.subjectSequelae
dc.subject.scopusOrganophosphate Poisoning; Nerve Agents; Tabun
dc.subject.wosEnvironmental sciences
dc.subject.wosPublic, environmental & occupational health
dc.titleBrain involvement in organophosphate poisoning
dc.typeArticle
dc.wos.quartileQ2 (Public, environmental & occupational health)
dc.wos.quartileQ1 (Public, environmental & occupational health)
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Anesteziyoloji ve Yoğun Bakım Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

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