dc.contributor.author |
Ng'ang'a, Zipporah W. |
|
dc.contributor.author |
Gicheru, Michael M. |
|
dc.contributor.author |
Namu, Samuel J. |
|
dc.date.accessioned |
2014-12-01T08:54:41Z |
|
dc.date.available |
2014-12-01T08:54:41Z |
|
dc.date.issued |
2013 |
|
dc.identifier.citation |
European International Journal of Science and Technology Vol. 2 No. 1 February 2013 |
en_US |
dc.identifier.uri |
www.cekinfo.org.uk/images/frontImages/gallery/Vol._2_No..._/7.pdf |
|
dc.identifier.uri |
http://hdl.handle.net/123456789/263 |
|
dc.description.abstract |
The objective of this study was to determine toxicity and immune status of HIV patients under ARVs
(Zidovudine, Stavudine and Nevirapine) which comprises first line ARV combination regime currently being
used in Kenya. A total of sixty (60) HIV patients participated in the study after consenting to undergo
comprehensive care. A control group of forty (40) HIV patients on only contrimoxale (septrin), Analysis of
Variance (ANOVA), t-test and correlation coeficient were used to analyse the data. The results showed
treatment with ARVs may cause . Based on the findings of this study it is recommended that the ARV drug
combination used may be initiated for patients at baseline CD4 counts of 101-150 cells/µl of blood. However
change to another ARV drug combination regime may be introduced after three months of use to minimize
toxicity associated with prolonged use. |
en_US |
dc.language.iso |
en |
en_US |
dc.subject |
Antiretrovirals |
en_US |
dc.subject |
Toxicity |
en_US |
dc.subject |
Immune status |
en_US |
dc.subject |
Creatinine |
en_US |
dc.title |
Antiretroviral drugs toxicity and immune status of HIV patients under comprehensive care in Embu, Kenya |
en_US |
dc.type |
Article |
en_US |