HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Cost-effectiveness of short-course zidovudine to prevent perinatal HIV type 1 infection in a sub-Saharan African Developing country setting.

AbstractOBJECTIVE:
To evaluate the cost-effectiveness of a short-course zidovudine program to prevent perinatal transmission of human immunodeficiency virus (HIV) type 1 in sub-Saharan African country settings.
DESIGN AND SETTING:
Several clinical trials of short-course zidovudine during pregnancy for prevention of perinatal transmission of HIV are under way in developing countries in sub-Saharan Africa. A decision model was used to examine the cost-effectiveness of zidovudine programs in a hypothetical 1-year birth cohort in a sub-Saharan African setting from the perspective of the health care system and of society. A completed short course of zidovudine was assumed to reduce perinatal HIV transmission from 25% to 16.5%, approximately one half of the effect of the longer-course zidovudine. Estimates of program costs, lifetime HIV-related health care costs, and lost productivity costs were derived from the published literature and from preliminary data available from sites of planned clinical trials. Sensitivity analyses were conducted on all relevant parameters.
MAIN OUTCOME MEASURES:
Medical costs, lost productivity costs, program costs, cost savings, and incremental cost-effectiveness, expressed as cost per infant HIV infection prevented.
RESULTS:
The model estimated that a national zidovudine program in a setting with 12.5% HIV seroprevalence would reduce perinatal HIV incidence by 12% (4.9 infections per 1000 births). The costs to the health care system would be $3748 per infant HIV infection prevented. When productivity losses were included in the model, the cost decreases to $1115 per infant HIV infection prevented. The cost to implement a national zidovudine program including the cost of counseling, testing, and drugs, would be $2 million per 100,000 births or $20 per pregnant woman. In the base case, decreases in the cost of counseling and testing and increases in maternal HIV prevalence, zidovudine efficacy, and medical and lost productivity costs improved cost-effectiveness of the zidovudine program.
CONCLUSIONS:
Assuming demonstrable efficacy of short-course zidovudine prevention of perinatal HIV, a national perinatal HIV prevention program with zidovudine in most sub-Saharan African country settings would reduce the incidence of infant HIV infection and, in some settings, provide societal savings; however, substantial initial investment in such programs will be required. Where health care resources are limited, as in these regions, allocation of resources to a perinatal zidovudine program will need to be considered in the context of resources required for other pressing medical care needs.
AuthorsG Mansergh, A C Haddix, R W Steketee, P I Nieburg, D J Hu, R J Simonds, M Rogers
JournalJAMA (JAMA) Vol. 276 Issue 2 Pg. 139-45 (Jul 10 1996) ISSN: 0098-7484 [Print] United States
PMID8656506 (Publication Type: Journal Article)
Chemical References
  • Antiviral Agents
  • Zidovudine
Topics
  • Africa South of the Sahara
  • Antiviral Agents (administration & dosage, economics, therapeutic use)
  • Cost-Benefit Analysis
  • Decision Support Techniques
  • Developing Countries (economics)
  • Female
  • HIV Infections (drug therapy, economics, prevention & control, transmission)
  • HIV-1
  • Humans
  • Infant, Newborn
  • Infectious Disease Transmission, Vertical (economics, prevention & control)
  • Multivariate Analysis
  • Pregnancy
  • Pregnancy Complications, Infectious (drug therapy, economics)
  • Program Development (economics)
  • Zidovudine (administration & dosage, economics, therapeutic use)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: