2007
DOI: 10.1097/01.inf.0000264527.69954.4c
|View full text |Cite
|
Sign up to set email alerts
|

Child Mortality According to Maternal and Infant HIV Status in Zimbabwe

Abstract: Perinatally infected infants are at particular risk of death between 2 and 6 months: cotrimoxazole prophylaxis and early pediatric HAART should be scaled up. Uninfected infants of infected mothers have at least twice the mortality risk of infants born to uninfected mothers: all HIV-exposed infants should be targeted with child survival interventions. HIV-positive mothers with more advanced disease are not only more likely to infect their infants, but their infants are more likely to die, whether infected or no… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

22
281
4

Year Published

2007
2007
2017
2017

Publication Types

Select...
5
3

Relationship

0
8

Authors

Journals

citations
Cited by 283 publications
(311 citation statements)
references
References 22 publications
22
281
4
Order By: Relevance
“…Our study was, however, limited by lack of HIV-1-unexposed, uninfected infants as controls. Immunologic abnormalities and increased rates of severe infections in HEU compared with HIV-unexposed infants have been described [13][14][15]. Furthermore, longitudinal assessment of the concentrations of plasma cytokines throughout the vaccination period to further assess changes in cytokines on ART and with sequential exposure to oral viral vaccine antigens was not performed due to sample availability.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Our study was, however, limited by lack of HIV-1-unexposed, uninfected infants as controls. Immunologic abnormalities and increased rates of severe infections in HEU compared with HIV-unexposed infants have been described [13][14][15]. Furthermore, longitudinal assessment of the concentrations of plasma cytokines throughout the vaccination period to further assess changes in cytokines on ART and with sequential exposure to oral viral vaccine antigens was not performed due to sample availability.…”
Section: Discussionmentioning
confidence: 99%
“…Cytokines commonly used to assess the inflammatory state in adult HIV-1 infection [7] 13], and tumor necrosis factor α [TNFα]) were quantified at study entry (prevaccination) and 21 days after the first vaccine dose using the ultrasensitive 10-plex human cytokine kit (V-Plex Proinflammatory Kit) from Meso-Scale Discoveries (Rockville, MD). Testing at additional time points was not performed due to lack of sample availability for the entire cohort.…”
Section: Quantitation Of Inflammation and Immune Activationmentioning
confidence: 99%
“…Cotrimoxazole, a highly effective antibiotic for preventing pneumonia and other opportunistic infections, and early paediatric antiretroviral treatment are fundamental for prolonging the lives of many infected infants. [20][21][22] Provision of cotrimoxazole prophylaxis for infants born to HIV positive mothers and HIV positive children has been slow in many countries. Cotrimoxazole can reduce child mortality in HIV positive children by over 40%, and has been part of the standard of care for preventing pneumonia and other opportunistic infections since the early 1990s.…”
Section: Global Progress On Paediatric Hiv Care and Treatment 2005mentioning
confidence: 99%
“…The severity of immunosuppression, and high viral loads in infants (23)(24)(25) are associated with rapid progression of HIV infection. On the contrary, maternal treatment even with prophylactic regimen, would indirectly reduce the progression of the disease in the infant (15,16,19,26). Some associated factors could be found in our milieu because of concurrent illness.…”
Section: Original Articlementioning
confidence: 99%
“…Rapid progressors are infants who develop severe signs of AIDS very early in life usually leading to death for most of them (13,14). Many factors are described in literature concerning HIV-infected rapid progressors (15)(16)(17)(18). It has been proven that there is a relationship between high maternal viral load and severe immunodeficiency, and high viral load in infants (15,(19)(20)(21)(22).…”
Section: Original Articlementioning
confidence: 99%