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dc.contributor.authorADERIBIGBE, A.-
dc.contributor.authorARIJE, A.-
dc.contributor.authorAKINKUGBE, O.O.-
dc.date.accessioned2022-01-17T09:16:52Z-
dc.date.available2022-01-17T09:16:52Z-
dc.date.issued1994-06-
dc.identifier.citationAfr. J. Med. Med. Sci. (1994). Vol 23. No 2: 153-160.en_US
dc.identifier.issn1116-4077-
dc.identifier.urihttp://adhlui.com.ui.edu.ng/jspui/handle/123456789/1753-
dc.description.abstractAn 8-month prospective study was carried out in 20 adult sickle cell disease (SCD) patients 16 sickle cell anaemia (Hbss) and 4 sickle cell Hbc disease (Hbsc); who had vaso-occlusive crises within the study period to determine the extent of the effect of sickle cell crisis on glomerular function in SCD patients during crises. The male: female ratio was 1: 5.7 and their mean age was 21.1 ± 7.9 years. Creatinine clearance (CCr), as an index of glomerular function, was determined at the pre-crisis, crisis, 2 and 4 weeks post-crisis and at the end of the study period. The mean values of their CCr dropped from 113.37 ± 33.80mliVmin at pre-crisis stage to 96.39 ± 30.13mls^min during crisis (p < 0.001) indicating glomerular dysfunction. It improved significantly to 107.75 ± 30.20mls/min at 4 weeks post-crisis (p < 0.001). There were no significant differences in the mean values of CCr at the end of the study (116.20 ± 31.43ml, Vmin) compared to the pre-crisis stage (p >0.05). It is concluded that glomerular dysfunction in SCD patients during crisis is potentially reversible.en_US
dc.description.sponsorshipCollege of Medicineen_US
dc.language.isoenen_US
dc.subjectSickle cellen_US
dc.subjectAnaemiaen_US
dc.subjectPatientsen_US
dc.subjectGlomerular functionen_US
dc.titleGlomerular function in sickle cell disease patients during crisisen_US
dc.typeArticleen_US
Appears in Collections:African Journal of Medicine and Medical Sciences

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