Implementation of HIV Early Infant Diagnosis and HIV Type 1 RNA Viral Load Determination on Dried Blood Spots in Cameroon: Challenges and Propositions

2012 ◽  
Vol 28 (2) ◽  
pp. 176-181 ◽  
Author(s):  
Céline Nguefeu Nkenfou ◽  
Elise Elong Lobé ◽  
Odile Ouwe-Missi-Oukem-Boyer ◽  
Martin Samuel Sosso ◽  
Béatrice Dambaya ◽  
...  
PLoS ONE ◽  
2014 ◽  
Vol 9 (3) ◽  
pp. e86461 ◽  
Author(s):  
Pieter W. Smit ◽  
Kimberly A. Sollis ◽  
Susan Fiscus ◽  
Nathan Ford ◽  
Marco Vitoria ◽  
...  

PLoS ONE ◽  
2017 ◽  
Vol 12 (6) ◽  
pp. e0179316 ◽  
Author(s):  
Clement Zeh ◽  
Kenneth Ndiege ◽  
Seth Inzaule ◽  
Rebecca Achieng ◽  
John Williamson ◽  
...  

PLoS ONE ◽  
2017 ◽  
Vol 12 (7) ◽  
pp. e0181352 ◽  
Author(s):  
Francisco Martin ◽  
Claudia Palladino ◽  
Rita Mateus ◽  
Anna Bolzan ◽  
Perpétua Gomes ◽  
...  

2010 ◽  
Vol 15 (7) ◽  
pp. 1003-1009 ◽  
Author(s):  
Asgeir Johannessen ◽  
Mona Holberg-Petersen ◽  
Gunilla Lövgaarden ◽  
Ezra Naman ◽  
Vidar Ormaasen ◽  
...  

2021 ◽  
Vol 8 (2) ◽  
pp. 136-144
Author(s):  
Aminat Omope Yusuf ◽  
Timothy Olugbenga Ogundeko ◽  
MamzhiSeljul Crown Ramyil ◽  
Catherine Nadabo ◽  
Nkiru Philomena Okoye

Early diagnosis of Human immunodeficiency virus (HIV) in infants provides a critical opportunity to strengthen follow-up of HIV- exposed children using dried blood spots and assure early access to antiretroviral treatment for infected children. This study aimed to determine the prevalence of HVI-1 infection in infants born to HIV-seropositive mothers. Early infant diagnosis of HIV sub-type I was carried out using on dried blood spots of 286 babies born to HIV-I seropositive mothers attending the Federal Medical Centre, Lokoja - Kogi State, Nigeria, between the months of July to December, 2013. Data obtained was analyzed using Gene Amp PCR System 9700. The overall rate of HIV-I vertical transmission from infected mothers to their babies was 14.5%. High transmission rates 63.5%was seen in babies whose mothers could not get any form of interventions with the least transmission rates seen in babies whose mothers either took HAART or were one form of ARV or the other (0 – 1.0%). Babies who took nevirapine as prophylaxis after delivery had lower rate (1%) of transmission. From the 30 women that mix-fed their babies, 6.7% transmission rate was recorded.Lack of antiretroviral drugs by HIV-I positive pregnant women was found to be associated with high rate of HIV-I transmission (p<0.05). Early intervention of mother to child transmission of HIV-1 infection using Highly Active Antiretroviral Therapy, exclusive breastfeeding practice as well as constant visit to Tertiary Hospitals for counseling and management of HIV infection reduced the rate of infection among the infants born to seropositive mothers.


2016 ◽  
Vol 229 ◽  
pp. 12-15 ◽  
Author(s):  
Sokhna Bousso Gueye ◽  
Halimatou Diop-Ndiaye ◽  
Mamadou Malick Diallo ◽  
Omar Ly ◽  
Aissatou Sow-Ndoye ◽  
...  

2014 ◽  
Vol 60 (4) ◽  
pp. 418-421 ◽  
Author(s):  
Julie A.E. Nelson ◽  
J. Tyler Hawkins ◽  
Maria Schanz ◽  
Katie Mollan ◽  
Melissa B. Miller ◽  
...  

2010 ◽  
Vol 2010 ◽  
pp. 1-6 ◽  
Author(s):  
Anders Persson ◽  
Charlotte Becker ◽  
Ida Hansson ◽  
Anita Nilsson ◽  
Carina Törn

To evaluate the performance of dried blood spots (DBSs) with subsequent analyses of glutamic acid decarboxylase (GADA) and islet antigen-2 (IA-2A) with the RSR-ELISAs, we selected 80 children newly diagnosed with type 1 diabetes and 120 healthy women. DBSs from patients and controls were used for RSR-ELISAs while patients samples were analysed also with in-house RIAs. The RSR-ELISA-GADA performed well with a specificity of 100%, albeit sensitivity (46%) was lower compared to in RIA (56%;P=.008). No prozone effect was observed after dilution of discrepant samples. RSR-ELISA-IA-2A achieved specificity of 69% and sensitivity was lower (59%) compared with RIA (66%;P<.001). Negative or low positive patients and control samples in the RSR-ELISA-IA-2A increased after dilution. Eluates from DBS can readily be used to analyse GADA with the RSR-ELISA, even if low levels of autoantibodies were not detected. Some factor could disturb RSR-ELISA-IA-2A analyses.


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