Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/21563
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dc.date.accessioned2021-08-31T06:44:08Z-
dc.date.available2021-08-31T06:44:08Z-
dc.date.issued1997-
dc.identifier.citationYılmazlar, A. ve Özyurt, G. (1997). "Brain involvement in organophosphate poisoning". Environmental Research, 74(2), 104-109.en_US
dc.identifier.issn0013-9351-
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.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.en_US
dc.language.isoenen_US
dc.publisherAcademic Press Inc Elsevier Scienceen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEnvironmental sciences & ecologyen_US
dc.subjectPublic, environmental & occupational healthen_US
dc.subjectBlood-flowen_US
dc.subjectIntoxicationen_US
dc.subjectNeurotoxicityen_US
dc.subjectNeuropathyen_US
dc.subjectMetabolismen_US
dc.subjectSequelaeen_US
dc.titleBrain involvement in organophosphate poisoningen_US
dc.typeArticleen_US
dc.identifier.wosA1997YC68600002tr_TR
dc.identifier.scopus2-s2.0-0031214468tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Anesteziyoloji ve Yoğun Bakım Anabilim Dalı.tr_TR
dc.identifier.startpage104tr_TR
dc.identifier.endpage109tr_TR
dc.identifier.volume74tr_TR
dc.identifier.issue2tr_TR
dc.relation.journalEnvironmental Researchen_US
dc.contributor.buuauthorYılmazlar, Aysun-
dc.contributor.buuauthorÖzyurt, Gürayten-
dc.identifier.pubmed9339222tr_TR
dc.subject.wosEnvironmental sciencesen_US
dc.subject.wosPublic, environmental & occupational healthen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ2 (Public, environmental & occupational health)en_US
dc.wos.quartileQ1 (Public, environmental & occupational health)en_US
dc.subject.scopusOrganophosphate Poisoning; Nerve Agents; Tabunen_US
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