dc.contributor.advisor | http://www.ncbi.nlm.nih.gov/pubmed/22824627 | |
dc.contributor.author | Maleche-Obimbo, E | |
dc.contributor.author | Overbaugh, J, | |
dc.contributor.author | Farquhar, C, | |
dc.contributor.author | Wamalwa, D, | |
dc.contributor.author | Richardson, BA, | |
dc.contributor.author | Tapia, KA, | |
dc.contributor.author | Slyker, JA, | |
dc.contributor.author | Diener, LC, | |
dc.date.accessioned | 2013-07-12T12:03:43Z | |
dc.date.available | 2013-07-12T12:03:43Z | |
dc.date.issued | 2012 | |
dc.identifier.citation | Diener LC, Slyker JA, GC, Tapia KA, Richardson BA, Wamalwa D, Farquhar C, Overbaugh J, Maleche-Obimbo E, G. J-S. 2012. Performance of the integrated management of childhood illness algorithm for diagnosis of HIV-1 infection among African infants. . AIDS. 2012 Sep 24;26(15):1935-41. . | en |
dc.identifier.uri | http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/47855 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/pubmed/22824627 | |
dc.identifier.uri | http://journals.lww.com/aidsonline/Fulltext/2012/09240/Performance_of_the_integrated_management_of.10.aspx | |
dc.description.abstract | OBJECTIVES:
Early infant HIV-1 diagnosis and treatment substantially improve survival. Where virologic HIV-1 testing is unavailable, integrated management of childhood illness (IMCI) clinical algorithms may be used for infant HIV-1 screening. We evaluated the performance of the 2008 WHO IMCI HIV algorithm in a cohort of HIV-exposed Kenyan infants.
METHODS:
From 1999 to 2003, 444 infants had monthly clinical assessments and quarterly virologic HIV-1 testing. Using archived clinical data, IMCI sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) were calculated using virologic testing as a gold standard. Linear regression and survival analyses were used to determine the effect of age on IMCI performance and timing of diagnosis.
RESULTS:
Overall IMCI sensitivity, specificity, PPV, and NPV value were 58, 87, 52, and 90%, respectively. Sensitivity (1.4%) and PPV (14%) were lowest at 1 month of age, when 81% of HIV infections already had occurred. Sensitivity increased with age (P < 0.0001), but remained low throughout infancy (range 1.4-35%). Specificity (range 97-100%) was high at each time point and was not associated with age. Fifty-eight percent of HIV-1-infected infants (50 of 86) were eventually diagnosed by IMCI, and use of IMCI was estimated to delay diagnosis in HIV-infected infants by a median of 5.9 months (P < 0.0001).
CONCLUSION:
IMCI had low sensitivity during the first month of life, when the majority of HIV-1 infections had already occurred and initiation of treatment is most critical. Although sensitivity increased with age, the substantial delay in HIV-1 diagnosis using IMCI limits its utility in early infant HIV-1 diagnosis. | en |
dc.language.iso | en | en |
dc.title | Performance of the integrated management of childhood illness algorithm for diagnosis of HIV-1 infection among African infants. | en |
dc.type | Article | en |
local.publisher | Department of of Paediatrics and Child health, University of Nairobi | en |