Matches in SemOpenAlex for { <https://semopenalex.org/work/W2894766171> ?p ?o ?g. }
- W2894766171 endingPage "e0204899" @default.
- W2894766171 startingPage "e0204899" @default.
- W2894766171 abstract "Introduction Iron deficiency anaemia (IDA) worsens the prognosis and outcomes of chronic kidney disease (CKD). However, while the haemoglobin level is unreliable for early detection of IDA, reticulocyte haemoglobin content (CHr) and hypochromic red cells (%HYPO) are early markers of IDA. Methods This was a cross sectional study of black adult participants (n = 258) with CKD and apparently healthy members of staff and patients’ relatives (n = 141) at the Charlotte Maxeke Johannesburg Academic Hospital, South Africa, between 1 June 2016 and 31 December 2016. Serum iron, serum ferritin and transferrin were measured using standard laboratory methods, while the haematology analyser was employed to measure CHr and %HYPO. The validity of CHr and %HYPO as markers of IDA were evaluated. Multivariable binary logistic regression was conducted to determine predictors of the relationship between IDA, CHr and %HYPO. The area under the receiver operator characteristics (ROC) curve (AUC) of the final models were utilised to evaluate the discriminatory value of CHr and %HYPO respectively. Results About one-quarter (26.1%) of the participants had IDA which was more than three times more frequent among CKD patients, compared to controls (35.3% vs 9.2%); 32.3% (95%CI: 27.90%– 37.10%) of the study population had iron deficiency without anaemia and the prevalence of iron deficiency without anaemia was lower in CKD patients compared to controls (29.5% vs 37.6%). The mean age of CKD patients was higher than in controls (52.7 ±14.3 vs 40.4 ±12.6 years, P-value<0.001). The sensitivity and specificity for diagnosing IDA among CKD participants was 62.6% and 80.2% respectively for CHr (at a cut-off value of <28pg) and 63.3% and 79.8% respectively for %HYPO. CKD participants with CHr levels >28pg were 82% less likely to be diagnosed as having IDA as compared to those with CHr levels ≤ 28pg) (adj odds ratio = 0.18, 95% CI: 0.09–0.37). The AUC of CHr (0.81, 95% CI: 0.76–0.87) was higher than the AUC of %HYPO (0.76, 95%CI: 0.70–0.82). Conclusion The diagnostic usefulness of CHr and the screening performance of %HYPO in predicting IDA among CKD patients are high. Their lower cost compared to conventional markers of ID recommend their use in clinical practice. Further cost effectiveness studies of these parameters are warranted." @default.
- W2894766171 created "2018-10-12" @default.
- W2894766171 creator A5018055193 @default.
- W2894766171 creator A5033306986 @default.
- W2894766171 creator A5038511561 @default.
- W2894766171 creator A5041234732 @default.
- W2894766171 creator A5044424784 @default.
- W2894766171 creator A5067532347 @default.
- W2894766171 creator A5087552786 @default.
- W2894766171 date "2018-10-03" @default.
- W2894766171 modified "2023-10-17" @default.
- W2894766171 title "Utility of reticulocyte haemoglobin content and percentage hypochromic red cells as markers of iron deficiency anaemia among black CKD patients in South Africa" @default.
- W2894766171 cites W1204102871 @default.
- W2894766171 cites W1986604740 @default.
- W2894766171 cites W1999017860 @default.
- W2894766171 cites W2016619456 @default.
- W2894766171 cites W2054100895 @default.
- W2894766171 cites W2076989190 @default.
- W2894766171 cites W2092348354 @default.
- W2894766171 cites W2099995173 @default.
- W2894766171 cites W2100474749 @default.
- W2894766171 cites W2102434796 @default.
- W2894766171 cites W2104444347 @default.
- W2894766171 cites W2120601666 @default.
- W2894766171 cites W2155965977 @default.
- W2894766171 cites W2166218331 @default.
- W2894766171 cites W2201635198 @default.
- W2894766171 cites W2212354254 @default.
- W2894766171 cites W2328387974 @default.
- W2894766171 cites W2607031541 @default.
- W2894766171 cites W2772301185 @default.
- W2894766171 cites W2790156897 @default.
- W2894766171 doi "https://doi.org/10.1371/journal.pone.0204899" @default.
- W2894766171 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6169908" @default.
- W2894766171 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30281654" @default.
- W2894766171 hasPublicationYear "2018" @default.
- W2894766171 type Work @default.
- W2894766171 sameAs 2894766171 @default.
- W2894766171 citedByCount "14" @default.
- W2894766171 countsByYear W28947661712019 @default.
- W2894766171 countsByYear W28947661712020 @default.
- W2894766171 countsByYear W28947661712021 @default.
- W2894766171 countsByYear W28947661712022 @default.
- W2894766171 countsByYear W28947661712023 @default.
- W2894766171 crossrefType "journal-article" @default.
- W2894766171 hasAuthorship W2894766171A5018055193 @default.
- W2894766171 hasAuthorship W2894766171A5033306986 @default.
- W2894766171 hasAuthorship W2894766171A5038511561 @default.
- W2894766171 hasAuthorship W2894766171A5041234732 @default.
- W2894766171 hasAuthorship W2894766171A5044424784 @default.
- W2894766171 hasAuthorship W2894766171A5067532347 @default.
- W2894766171 hasAuthorship W2894766171A5087552786 @default.
- W2894766171 hasBestOaLocation W28947661711 @default.
- W2894766171 hasConcept C104317684 @default.
- W2894766171 hasConcept C105580179 @default.
- W2894766171 hasConcept C126322002 @default.
- W2894766171 hasConcept C153852466 @default.
- W2894766171 hasConcept C187212893 @default.
- W2894766171 hasConcept C2777417653 @default.
- W2894766171 hasConcept C2778248108 @default.
- W2894766171 hasConcept C2778319317 @default.
- W2894766171 hasConcept C2778403015 @default.
- W2894766171 hasConcept C2778653478 @default.
- W2894766171 hasConcept C2780959883 @default.
- W2894766171 hasConcept C2908647359 @default.
- W2894766171 hasConcept C55493867 @default.
- W2894766171 hasConcept C58471807 @default.
- W2894766171 hasConcept C71924100 @default.
- W2894766171 hasConcept C86803240 @default.
- W2894766171 hasConcept C90924648 @default.
- W2894766171 hasConcept C99454951 @default.
- W2894766171 hasConceptScore W2894766171C104317684 @default.
- W2894766171 hasConceptScore W2894766171C105580179 @default.
- W2894766171 hasConceptScore W2894766171C126322002 @default.
- W2894766171 hasConceptScore W2894766171C153852466 @default.
- W2894766171 hasConceptScore W2894766171C187212893 @default.
- W2894766171 hasConceptScore W2894766171C2777417653 @default.
- W2894766171 hasConceptScore W2894766171C2778248108 @default.
- W2894766171 hasConceptScore W2894766171C2778319317 @default.
- W2894766171 hasConceptScore W2894766171C2778403015 @default.
- W2894766171 hasConceptScore W2894766171C2778653478 @default.
- W2894766171 hasConceptScore W2894766171C2780959883 @default.
- W2894766171 hasConceptScore W2894766171C2908647359 @default.
- W2894766171 hasConceptScore W2894766171C55493867 @default.
- W2894766171 hasConceptScore W2894766171C58471807 @default.
- W2894766171 hasConceptScore W2894766171C71924100 @default.
- W2894766171 hasConceptScore W2894766171C86803240 @default.
- W2894766171 hasConceptScore W2894766171C90924648 @default.
- W2894766171 hasConceptScore W2894766171C99454951 @default.
- W2894766171 hasIssue "10" @default.
- W2894766171 hasLocation W28947661711 @default.
- W2894766171 hasLocation W28947661712 @default.
- W2894766171 hasLocation W28947661713 @default.
- W2894766171 hasLocation W28947661714 @default.
- W2894766171 hasLocation W28947661715 @default.
- W2894766171 hasOpenAccess W2894766171 @default.
- W2894766171 hasPrimaryLocation W28947661711 @default.
- W2894766171 hasRelatedWork W2156498798 @default.