Objectives:
To determine the
incidence and risk factors of mortality for all HIV-infected patients receiving
antiretroviral treatment at public and private healthcare facilities in the
Botswana National HIV/AIDS Treatment Programme.
Design:
We studied routinely
collected data from 226 030 patients enrolled in the Botswana National HIV/AIDS
Treatment Programme from 2002 to 2013.
Methods:
A person-years (P-Y)
approach was used to analyse all-cause mortality and follow-up rates for all
HIV-infected individuals with documented antiretroviral therapy initiation
dates. Marginal structural modelling was utilized to determine the effect of
treatment on survival for those with documented drug regimens. Sensitivity
analyses were performed to assess the robustness of our results.
Results:
Median follow-up time
was 37 months (interquartile range 11–75). Mortality was highest during the
first 3 months after treatment initiation at 11.79 (95% confidence interval
11.49–12.11) deaths per 100 P-Y, but dropped to 1.01 (95% confidence interval
0.98–1.04) deaths per 100 P-Y after the first year of treatment. Twelve-month
mortality declined from 7 to 2% of initiates during 2002–2012. Tenofovir was
associated with lower mortality than stavudine and zidovudine.
Conclusion:
The observed mortality
rates have been declining over time; however, mortality in the first year,
particularly first 3 months of antiretroviral treatment, remains a distinct
problem. This analysis showed lower mortality with regimens containing
tenofovir compared with zidovudine and stavudine. CD4+ cell count less than 100 cells/μl, older age and being male
were associated with higher odds of mortality.
Below: Distribution of yearly deaths by duration of treatment.
Below: Mortality rate in the first year after treatment initiation
By: Mansour Farahani,a Natalie Price,a Shenaaz El-Halabi,b Naledi Mlaudzi,b Koona Keapoletswe,b Refeletswe Lebelonyane,b Ernest Benny Fetogang,b Tony Chebani,a Poloko Kebaabetswe,c Tiny Masupe,c Keba Gabaake,c Andrew Auld,d Oathokwa Nkomazana,c and Richard Marlinka
aHarvard T.H. Chan School of Public Health,
Boston, Massachusetts, USA
bMinistry of Health
cUniversity of Botswana, Gaborone, Botswana
dCenter for Disease Control and Prevention,
Atlanta, Georgia, USA.
Correspondence to Mansour Farahani, MD, MPH, ScD, Harvard
School of Public Health, Boston, MA, USA. E-mail:
AIDS. 2016 Jan 28; 30(3): 477–485.
More at: https://twitter.com/hiv insight
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