2004
DOI: 10.1590/s0004-282x2004000500030
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Hemorrhagic stroke after naphazoline exposition: case report

Abstract: -Ten percent of all strokes are due to spontaneous cerebral hemorrhages. They are associated to drugs (licit and illicit) in 9.5% of all cases in young adults. This is a case report of a 44-year-old man, without previous morbidities, who presented a sudden onset headache and arterial hypertension 24 hours after use of naphazoline as nasal decongestant. Cranial tomography showed right thalamus hemorrhage. Cerebral angiography showed no aneurisms, vascular malformations or vasculitis. No other risk factors were … Show more

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Cited by 16 publications
(14 citation statements)
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“…По мимо восстановления носового дыхания эти препа раты не оказывают никакого действия на другие симптомы ринита: они не уменьшают количество чиханий, а экспериментальные исследования на животных показывают, что при лечении вазокон стрикторами количество выделений из носа даже увеличивается [17]. [18,19], и даже приводить к ишемиче ским и геморрагическим инсультам головного мозга [20,21].…”
Section: показанияunclassified
“…По мимо восстановления носового дыхания эти препа раты не оказывают никакого действия на другие симптомы ринита: они не уменьшают количество чиханий, а экспериментальные исследования на животных показывают, что при лечении вазокон стрикторами количество выделений из носа даже увеличивается [17]. [18,19], и даже приводить к ишемиче ским и геморрагическим инсультам головного мозга [20,21].…”
Section: показанияunclassified
“…The present study describes the use of 6-carbethoxy-3,5-diarylcyclohex-2-enone 23 as a key intermediate with three versative functional groups i.e., ketone, olefin, and ester for the synthesis of imidazolidine derivatives. Owing to our interest in synthesis of fascinating biologically active hybrid heterocyclic compounds [24][25][26] and as part of our research program, herein we planned to design a spiro imidazolidine derivatives bearing a cyclohexene substituent on the carbon between the nitrogen centers to give a new series of spiro imidazolidine heterocycles because most bio-active imidazolidine derivatives bear a substituent (aryl or alkyl group) on the carbon between the nitrogen centers [18][19][20][21] .…”
Section: Original Articlementioning
confidence: 99%
“…This serves to relieve the redness of the eye caused by minor ocular irritants. Naphazoline is a sympathomimetic agent 20 with marked α-adrenergic activity. Clonidine is used as a direct-acting α-2 adrenergic agonist.…”
Section: Introductionmentioning
confidence: 99%
“…This serves to relieve the redness of the eye caused by minor ocular irritants. Naphazoline is a sympathomimetic agent [11] with marked α-adrenergic activity. It is a vasoconstrictor with a rapid action in reducing swelling when applied to mucous membrane.…”
mentioning
confidence: 99%
“…The present study describes the use of ethyl 4,6-diaryl-2-oxocyclohex-3-ene-1-carboxylates [21], intermediates with three versatile functional groups, i.e., ketone, olefin, and ester, for the synthesis of imidazoline derivatives. In continuation of our earlier work on the synthesis of structurally diverse biologically active hybrid heterocyclic ring systems and as part of our ongoing research program [22][23][24][25][26], we plan to design imidazoline derivatives bearing a cyclohexene substituent bound by a spiro-linkage to the carbon atom between the nitrogen centers to obtain a new series of heterocycles, namely, ethyl 7,9-diaryl-1,4-diazaspiro [4.5]dec-9-ene-6-carboxylates since most of the bioactive imidazoline derivatives bear a substituent (aryl or alkyl group) on this carbon center [11][12][13]. In order to evaluate the effect of the structure on the biological activity of the target compounds, we chose different substituents at the phenyl rings of the starting reactants.…”
mentioning
confidence: 99%